Canonical Allele Identifier: CA351204646

Gene: LRRFIP1

Linked Data

• MyVariant Identifiers: chr2:g.238672552A>T (hg19) ; chr2:g.237763909A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763909A>T , CM000664.2:g.237763909A>T	GRCh38
NC_000002.11:g.238672552A>T , CM000664.1:g.238672552A>T	GRCh37
NC_000002.10:g.238337291A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3704A>T
ENST00000698098.1:c.955+3704A>T	ENSP00000513562.1:n.955+3704A>T
ENST00000308482.14:c.1459+3704A>T MANE Select	ENSP00000310109.9:n.1459+3704A>T
ENST00000244815.9:c.2124A>T	ENSP00000244815.5:p.Glu708Asp
ENST00000289175.10:c.2028A>T	ENSP00000289175.6:p.Glu676Asp
ENST00000308482.13:c.1459+3704A>T	ENSP00000310109.9:n.1459+3704A>T
ENST00000392000.4:c.2196A>T	ENSP00000375857.4:p.Glu732Asp
ENST00000483443.1:n.235+3704A>T
NM_001137550.1:c.1459+3704A>T	NP_001131022.1:n.1459+3704A>T
NM_001137551.1:c.721+3704A>T	NP_001131023.1:n.721+3704A>T
NM_001137552.1:c.2196A>T	NP_001131024.1:p.Glu732Asp
NM_001137553.1:c.2028A>T	NP_001131025.1:p.Glu676Asp
NM_004735.3:c.2124A>T	NP_004726.2:p.Glu708Asp
XM_005246112.3:c.2829A>T	XP_005246169.1:p.Glu943Asp
XM_005246115.3:c.2784A>T	XP_005246172.1:p.Glu928Asp
XM_005246116.3:c.2766A>T	XP_005246173.1:p.Glu922Asp
XM_005246118.3:c.2721A>T	XP_005246175.1:p.Glu907Asp
XM_005246119.3:c.2718A>T	XP_005246176.1:p.Glu906Asp
XM_005246120.3:c.2682A>T	XP_005246177.1:p.Glu894Asp
XM_005246121.3:c.2667A>T	XP_005246178.1:p.Glu889Asp
XM_005246122.3:c.2655A>T	XP_005246179.1:p.Glu885Asp
XM_005246124.1:c.2637A>T	XP_005246181.1:p.Glu879Asp
XM_005246125.3:c.2616A>T	XP_005246182.1:p.Glu872Asp
XM_005246126.3:c.2577A>T	XP_005246183.1:p.Glu859Asp
XM_005246128.1:c.2544A>T	XP_005246185.1:p.Glu848Asp
XM_005246129.3:c.2505A>T	XP_005246186.1:p.Glu835Asp
XM_005246130.3:c.2478A>T	XP_005246187.1:p.Glu826Asp
XM_005246131.3:c.2391A>T	XP_005246188.1:p.Glu797Asp
XM_005246132.3:c.2316A>T	XP_005246189.1:p.Glu772Asp
XM_005246133.1:c.2286A>T	XP_005246190.1:p.Glu762Asp
XM_005246134.1:c.2244A>T	XP_005246191.1:p.Glu748Asp
XM_005246135.1:c.2214A>T	XP_005246192.1:p.Glu738Asp
XM_005246136.1:c.2058A>T	XP_005246193.1:p.Glu686Asp
XM_005246141.3:c.823+3704A>T	XP_005246198.1:n.823+3704A>T
XM_005246142.1:c.751+3704A>T	XP_005246199.1:n.751+3704A>T
XM_006712842.2:c.2727A>T	XP_006712905.1:p.Glu909Asp
XM_006712843.2:c.2622A>T	XP_006712906.1:p.Glu874Asp
XM_006712844.1:c.2556A>T	XP_006712907.1:p.Glu852Asp
XM_006712845.2:c.2538A>T	XP_006712908.1:p.Glu846Asp
XM_006712846.1:c.2442A>T	XP_006712909.1:p.Glu814Asp
XM_006712847.1:c.2382A>T	XP_006712910.1:p.Glu794Asp
XM_006712848.1:c.2310A>T	XP_006712911.1:p.Glu770Asp
XM_011512152.1:c.2862A>T	XP_011510454.1:p.Glu954Asp
XM_011512153.1:c.2844A>T	XP_011510455.1:p.Glu948Asp
XM_011512154.1:c.2832A>T	XP_011510456.1:p.Glu944Asp
XM_011512155.1:c.2823A>T	XP_011510457.1:p.Glu941Asp
XM_011512156.1:c.2790A>T	XP_011510458.1:p.Glu930Asp
XM_011512157.1:c.2676A>T	XP_011510459.1:p.Glu892Asp
XM_011512158.1:c.2604A>T	XP_011510460.1:p.Glu868Asp
XM_011512159.1:c.2412A>T	XP_011510461.1:p.Glu804Asp
XM_011512160.1:c.1555+3704A>T	XP_011510462.1:n.1555+3704A>T
XM_011512161.1:c.1555+3704A>T	XP_011510463.1:n.1555+3704A>T
XM_011512162.1:c.1369+3704A>T	XP_011510464.1:n.1369+3704A>T
XM_011512163.1:c.1297+3704A>T	XP_011510465.1:n.1297+3704A>T
XM_011512164.1:c.751+3704A>T	XP_011510466.1:n.751+3704A>T
XM_011512165.1:c.721+3704A>T	XP_011510467.1:n.721+3704A>T
XM_011512166.1:c.1516+3704A>T	XP_011510468.1:n.1516+3704A>T
XR_923063.1:n.1605+3704A>T
XM_005246141.4:c.823+3704A>T	XP_005246198.1:n.823+3704A>T
XM_005246142.2:c.751+3704A>T	XP_005246199.1:n.751+3704A>T
XM_017005253.2:c.1522+3704A>T	XP_016860742.1:n.1522+3704A>T
XM_017005254.2:c.1522+3704A>T	XP_016860743.1:n.1522+3704A>T
XM_017005255.2:c.1450+3704A>T	XP_016860744.1:n.1450+3704A>T
XM_017005256.2:c.1336+3704A>T	XP_016860745.1:n.1336+3704A>T
XM_017005257.2:c.1387+3704A>T	XP_016860746.1:n.1387+3704A>T
XM_017005258.2:c.1336+3704A>T	XP_016860747.1:n.1336+3704A>T
XM_017005260.2:c.1162+3704A>T	XP_016860749.1:n.1162+3704A>T
XM_017005261.2:c.1099+3704A>T	XP_016860750.1:n.1099+3704A>T
XM_017005262.2:c.1099+3704A>T	XP_016860751.1:n.1099+3704A>T
XM_017005263.2:c.937+3704A>T	XP_016860752.1:n.937+3704A>T
XR_001739039.2:n.2898A>T
XR_001739040.1:n.3063A>T
XR_001739041.2:n.2859A>T
XR_001739042.2:n.2835A>T
XR_001739043.1:n.2811A>T
XR_001739044.2:n.2826A>T
XR_001739045.2:n.2796A>T
XR_001739046.1:n.3143A>T
XR_001739047.2:n.2712A>T
XR_001739048.1:n.2901A>T
XR_001739049.2:n.2646A>T
XR_001739050.2:n.2607A>T
XR_001739051.2:n.2574A>T
XR_001739052.2:n.2547A>T
XR_001739053.1:n.2536A>T
XR_001739054.1:n.2458A>T
XR_001739055.2:n.2475A>T
XR_001739056.2:n.2460A>T
XR_001739057.1:n.2476A>T
XR_001739058.1:n.2655A>T
XR_001739059.2:n.2388A>T
XR_001739060.1:n.2362A>T
XR_001739061.1:n.2404A>T
XR_001739062.1:n.2581A>T
XR_001739063.1:n.2288A>T
XR_001739064.1:n.2549A>T
XR_001739065.1:n.2493A>T
XR_001739066.1:n.2290A>T
XR_001739067.1:n.2197A>T
XR_001739068.1:n.2218A>T
XR_001739069.1:n.2395A>T
XR_001739070.1:n.2259A>T
XR_001739071.1:n.2117A>T
XR_001739072.1:n.2363A>T
XR_001739073.2:n.1591+3704A>T
XR_002959364.1:n.2289A>T
NM_001137550.2:c.1459+3704A>T MANE Select	NP_001131022.1:n.1459+3704A>T
NM_001137552.2:c.2196A>T	NP_001131024.1:p.Glu732Asp
NM_001137553.2:c.2028A>T	NP_001131025.1:p.Glu676Asp
NM_004735.4:c.2124A>T	NP_004726.2:p.Glu708Asp
NM_001137551.2:c.721+3704A>T	NP_001131023.1:n.721+3704A>T