Canonical Allele Identifier: CA351204155

Gene: LRRFIP1

Linked Data

• MyVariant Identifiers: chr2:g.238672480T>G (hg19) ; chr2:g.237763837T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763837T>G , CM000664.2:g.237763837T>G	GRCh38
NC_000002.11:g.238672480T>G , CM000664.1:g.238672480T>G	GRCh37
NC_000002.10:g.238337219T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3632T>G
ENST00000698098.1:c.955+3632T>G	ENSP00000513562.1:n.955+3632T>G
ENST00000308482.14:c.1459+3632T>G MANE Select	ENSP00000310109.9:n.1459+3632T>G
ENST00000244815.9:c.2052T>G	ENSP00000244815.5:p.Asp684Glu
ENST00000289175.10:c.1956T>G	ENSP00000289175.6:p.Asp652Glu
ENST00000308482.13:c.1459+3632T>G	ENSP00000310109.9:n.1459+3632T>G
ENST00000392000.4:c.2124T>G	ENSP00000375857.4:p.Asp708Glu
ENST00000483443.1:n.235+3632T>G
NM_001137550.1:c.1459+3632T>G	NP_001131022.1:n.1459+3632T>G
NM_001137551.1:c.721+3632T>G	NP_001131023.1:n.721+3632T>G
NM_001137552.1:c.2124T>G	NP_001131024.1:p.Asp708Glu
NM_001137553.1:c.1956T>G	NP_001131025.1:p.Asp652Glu
NM_004735.3:c.2052T>G	NP_004726.2:p.Asp684Glu
XM_005246112.3:c.2757T>G	XP_005246169.1:p.Asp919Glu
XM_005246115.3:c.2712T>G	XP_005246172.1:p.Asp904Glu
XM_005246116.3:c.2694T>G	XP_005246173.1:p.Asp898Glu
XM_005246118.3:c.2649T>G	XP_005246175.1:p.Asp883Glu
XM_005246119.3:c.2646T>G	XP_005246176.1:p.Asp882Glu
XM_005246120.3:c.2610T>G	XP_005246177.1:p.Asp870Glu
XM_005246121.3:c.2595T>G	XP_005246178.1:p.Asp865Glu
XM_005246122.3:c.2583T>G	XP_005246179.1:p.Asp861Glu
XM_005246124.1:c.2565T>G	XP_005246181.1:p.Asp855Glu
XM_005246125.3:c.2544T>G	XP_005246182.1:p.Asp848Glu
XM_005246126.3:c.2505T>G	XP_005246183.1:p.Asp835Glu
XM_005246128.1:c.2472T>G	XP_005246185.1:p.Asp824Glu
XM_005246129.3:c.2433T>G	XP_005246186.1:p.Asp811Glu
XM_005246130.3:c.2406T>G	XP_005246187.1:p.Asp802Glu
XM_005246131.3:c.2319T>G	XP_005246188.1:p.Asp773Glu
XM_005246132.3:c.2244T>G	XP_005246189.1:p.Asp748Glu
XM_005246133.1:c.2214T>G	XP_005246190.1:p.Asp738Glu
XM_005246134.1:c.2172T>G	XP_005246191.1:p.Asp724Glu
XM_005246135.1:c.2142T>G	XP_005246192.1:p.Asp714Glu
XM_005246136.1:c.1986T>G	XP_005246193.1:p.Asp662Glu
XM_005246141.3:c.823+3632T>G	XP_005246198.1:n.823+3632T>G
XM_005246142.1:c.751+3632T>G	XP_005246199.1:n.751+3632T>G
XM_006712842.2:c.2655T>G	XP_006712905.1:p.Asp885Glu
XM_006712843.2:c.2550T>G	XP_006712906.1:p.Asp850Glu
XM_006712844.1:c.2484T>G	XP_006712907.1:p.Asp828Glu
XM_006712845.2:c.2466T>G	XP_006712908.1:p.Asp822Glu
XM_006712846.1:c.2370T>G	XP_006712909.1:p.Asp790Glu
XM_006712847.1:c.2310T>G	XP_006712910.1:p.Asp770Glu
XM_006712848.1:c.2238T>G	XP_006712911.1:p.Asp746Glu
XM_011512152.1:c.2790T>G	XP_011510454.1:p.Asp930Glu
XM_011512153.1:c.2772T>G	XP_011510455.1:p.Asp924Glu
XM_011512154.1:c.2760T>G	XP_011510456.1:p.Asp920Glu
XM_011512155.1:c.2751T>G	XP_011510457.1:p.Asp917Glu
XM_011512156.1:c.2718T>G	XP_011510458.1:p.Asp906Glu
XM_011512157.1:c.2604T>G	XP_011510459.1:p.Asp868Glu
XM_011512158.1:c.2532T>G	XP_011510460.1:p.Asp844Glu
XM_011512159.1:c.2340T>G	XP_011510461.1:p.Asp780Glu
XM_011512160.1:c.1555+3632T>G	XP_011510462.1:n.1555+3632T>G
XM_011512161.1:c.1555+3632T>G	XP_011510463.1:n.1555+3632T>G
XM_011512162.1:c.1369+3632T>G	XP_011510464.1:n.1369+3632T>G
XM_011512163.1:c.1297+3632T>G	XP_011510465.1:n.1297+3632T>G
XM_011512164.1:c.751+3632T>G	XP_011510466.1:n.751+3632T>G
XM_011512165.1:c.721+3632T>G	XP_011510467.1:n.721+3632T>G
XM_011512166.1:c.1516+3632T>G	XP_011510468.1:n.1516+3632T>G
XR_923063.1:n.1605+3632T>G
XM_005246141.4:c.823+3632T>G	XP_005246198.1:n.823+3632T>G
XM_005246142.2:c.751+3632T>G	XP_005246199.1:n.751+3632T>G
XM_017005253.2:c.1522+3632T>G	XP_016860742.1:n.1522+3632T>G
XM_017005254.2:c.1522+3632T>G	XP_016860743.1:n.1522+3632T>G
XM_017005255.2:c.1450+3632T>G	XP_016860744.1:n.1450+3632T>G
XM_017005256.2:c.1336+3632T>G	XP_016860745.1:n.1336+3632T>G
XM_017005257.2:c.1387+3632T>G	XP_016860746.1:n.1387+3632T>G
XM_017005258.2:c.1336+3632T>G	XP_016860747.1:n.1336+3632T>G
XM_017005260.2:c.1162+3632T>G	XP_016860749.1:n.1162+3632T>G
XM_017005261.2:c.1099+3632T>G	XP_016860750.1:n.1099+3632T>G
XM_017005262.2:c.1099+3632T>G	XP_016860751.1:n.1099+3632T>G
XM_017005263.2:c.937+3632T>G	XP_016860752.1:n.937+3632T>G
XR_001739039.2:n.2826T>G
XR_001739040.1:n.2991T>G
XR_001739041.2:n.2787T>G
XR_001739042.2:n.2763T>G
XR_001739043.1:n.2739T>G
XR_001739044.2:n.2754T>G
XR_001739045.2:n.2724T>G
XR_001739046.1:n.3071T>G
XR_001739047.2:n.2640T>G
XR_001739048.1:n.2829T>G
XR_001739049.2:n.2574T>G
XR_001739050.2:n.2535T>G
XR_001739051.2:n.2502T>G
XR_001739052.2:n.2475T>G
XR_001739053.1:n.2464T>G
XR_001739054.1:n.2386T>G
XR_001739055.2:n.2403T>G
XR_001739056.2:n.2388T>G
XR_001739057.1:n.2404T>G
XR_001739058.1:n.2583T>G
XR_001739059.2:n.2316T>G
XR_001739060.1:n.2290T>G
XR_001739061.1:n.2332T>G
XR_001739062.1:n.2509T>G
XR_001739063.1:n.2216T>G
XR_001739064.1:n.2477T>G
XR_001739065.1:n.2421T>G
XR_001739066.1:n.2218T>G
XR_001739067.1:n.2125T>G
XR_001739068.1:n.2146T>G
XR_001739069.1:n.2323T>G
XR_001739070.1:n.2187T>G
XR_001739071.1:n.2045T>G
XR_001739072.1:n.2291T>G
XR_001739073.2:n.1591+3632T>G
XR_002959364.1:n.2217T>G
NM_001137550.2:c.1459+3632T>G MANE Select	NP_001131022.1:n.1459+3632T>G
NM_001137552.2:c.2124T>G	NP_001131024.1:p.Asp708Glu
NM_001137553.2:c.1956T>G	NP_001131025.1:p.Asp652Glu
NM_004735.4:c.2052T>G	NP_004726.2:p.Asp684Glu
NM_001137551.2:c.721+3632T>G	NP_001131023.1:n.721+3632T>G