Canonical Allele Identifier: CA351204715

Gene: LRRFIP1

Linked Data

• MyVariant Identifiers: chr2:g.238672569T>G (hg19) ; chr2:g.237763926T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763926T>G , CM000664.2:g.237763926T>G	GRCh38
NC_000002.11:g.238672569T>G , CM000664.1:g.238672569T>G	GRCh37
NC_000002.10:g.238337308T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3721T>G
ENST00000698098.1:c.955+3721T>G	ENSP00000513562.1:n.955+3721T>G
ENST00000308482.14:c.1459+3721T>G MANE Select	ENSP00000310109.9:n.1459+3721T>G
ENST00000244815.9:c.2141T>G	ENSP00000244815.5:p.Ile714Ser
ENST00000289175.10:c.2045T>G	ENSP00000289175.6:p.Ile682Ser
ENST00000308482.13:c.1459+3721T>G	ENSP00000310109.9:n.1459+3721T>G
ENST00000392000.4:c.2213T>G	ENSP00000375857.4:p.Ile738Ser
ENST00000483443.1:n.235+3721T>G
NM_001137550.1:c.1459+3721T>G	NP_001131022.1:n.1459+3721T>G
NM_001137551.1:c.721+3721T>G	NP_001131023.1:n.721+3721T>G
NM_001137552.1:c.2213T>G	NP_001131024.1:p.Ile738Ser
NM_001137553.1:c.2045T>G	NP_001131025.1:p.Ile682Ser
NM_004735.3:c.2141T>G	NP_004726.2:p.Ile714Ser
XM_005246112.3:c.2846T>G	XP_005246169.1:p.Ile949Ser
XM_005246115.3:c.2801T>G	XP_005246172.1:p.Ile934Ser
XM_005246116.3:c.2783T>G	XP_005246173.1:p.Ile928Ser
XM_005246118.3:c.2738T>G	XP_005246175.1:p.Ile913Ser
XM_005246119.3:c.2735T>G	XP_005246176.1:p.Ile912Ser
XM_005246120.3:c.2699T>G	XP_005246177.1:p.Ile900Ser
XM_005246121.3:c.2684T>G	XP_005246178.1:p.Ile895Ser
XM_005246122.3:c.2672T>G	XP_005246179.1:p.Ile891Ser
XM_005246124.1:c.2654T>G	XP_005246181.1:p.Ile885Ser
XM_005246125.3:c.2633T>G	XP_005246182.1:p.Ile878Ser
XM_005246126.3:c.2594T>G	XP_005246183.1:p.Ile865Ser
XM_005246128.1:c.2561T>G	XP_005246185.1:p.Ile854Ser
XM_005246129.3:c.2522T>G	XP_005246186.1:p.Ile841Ser
XM_005246130.3:c.2495T>G	XP_005246187.1:p.Ile832Ser
XM_005246131.3:c.2408T>G	XP_005246188.1:p.Ile803Ser
XM_005246132.3:c.2333T>G	XP_005246189.1:p.Ile778Ser
XM_005246133.1:c.2303T>G	XP_005246190.1:p.Ile768Ser
XM_005246134.1:c.2261T>G	XP_005246191.1:p.Ile754Ser
XM_005246135.1:c.2231T>G	XP_005246192.1:p.Ile744Ser
XM_005246136.1:c.2075T>G	XP_005246193.1:p.Ile692Ser
XM_005246141.3:c.823+3721T>G	XP_005246198.1:n.823+3721T>G
XM_005246142.1:c.751+3721T>G	XP_005246199.1:n.751+3721T>G
XM_006712842.2:c.2744T>G	XP_006712905.1:p.Ile915Ser
XM_006712843.2:c.2639T>G	XP_006712906.1:p.Ile880Ser
XM_006712844.1:c.2573T>G	XP_006712907.1:p.Ile858Ser
XM_006712845.2:c.2555T>G	XP_006712908.1:p.Ile852Ser
XM_006712846.1:c.2459T>G	XP_006712909.1:p.Ile820Ser
XM_006712847.1:c.2399T>G	XP_006712910.1:p.Ile800Ser
XM_006712848.1:c.2327T>G	XP_006712911.1:p.Ile776Ser
XM_011512152.1:c.2879T>G	XP_011510454.1:p.Ile960Ser
XM_011512153.1:c.2861T>G	XP_011510455.1:p.Ile954Ser
XM_011512154.1:c.2849T>G	XP_011510456.1:p.Ile950Ser
XM_011512155.1:c.2840T>G	XP_011510457.1:p.Ile947Ser
XM_011512156.1:c.2807T>G	XP_011510458.1:p.Ile936Ser
XM_011512157.1:c.2693T>G	XP_011510459.1:p.Ile898Ser
XM_011512158.1:c.2621T>G	XP_011510460.1:p.Ile874Ser
XM_011512159.1:c.2429T>G	XP_011510461.1:p.Ile810Ser
XM_011512160.1:c.1555+3721T>G	XP_011510462.1:n.1555+3721T>G
XM_011512161.1:c.1555+3721T>G	XP_011510463.1:n.1555+3721T>G
XM_011512162.1:c.1369+3721T>G	XP_011510464.1:n.1369+3721T>G
XM_011512163.1:c.1297+3721T>G	XP_011510465.1:n.1297+3721T>G
XM_011512164.1:c.751+3721T>G	XP_011510466.1:n.751+3721T>G
XM_011512165.1:c.721+3721T>G	XP_011510467.1:n.721+3721T>G
XM_011512166.1:c.1516+3721T>G	XP_011510468.1:n.1516+3721T>G
XR_923063.1:n.1605+3721T>G
XM_005246141.4:c.823+3721T>G	XP_005246198.1:n.823+3721T>G
XM_005246142.2:c.751+3721T>G	XP_005246199.1:n.751+3721T>G
XM_017005253.2:c.1522+3721T>G	XP_016860742.1:n.1522+3721T>G
XM_017005254.2:c.1522+3721T>G	XP_016860743.1:n.1522+3721T>G
XM_017005255.2:c.1450+3721T>G	XP_016860744.1:n.1450+3721T>G
XM_017005256.2:c.1336+3721T>G	XP_016860745.1:n.1336+3721T>G
XM_017005257.2:c.1387+3721T>G	XP_016860746.1:n.1387+3721T>G
XM_017005258.2:c.1336+3721T>G	XP_016860747.1:n.1336+3721T>G
XM_017005260.2:c.1162+3721T>G	XP_016860749.1:n.1162+3721T>G
XM_017005261.2:c.1099+3721T>G	XP_016860750.1:n.1099+3721T>G
XM_017005262.2:c.1099+3721T>G	XP_016860751.1:n.1099+3721T>G
XM_017005263.2:c.937+3721T>G	XP_016860752.1:n.937+3721T>G
XR_001739039.2:n.2915T>G
XR_001739040.1:n.3080T>G
XR_001739041.2:n.2876T>G
XR_001739042.2:n.2852T>G
XR_001739043.1:n.2828T>G
XR_001739044.2:n.2843T>G
XR_001739045.2:n.2813T>G
XR_001739046.1:n.3160T>G
XR_001739047.2:n.2729T>G
XR_001739048.1:n.2918T>G
XR_001739049.2:n.2663T>G
XR_001739050.2:n.2624T>G
XR_001739051.2:n.2591T>G
XR_001739052.2:n.2564T>G
XR_001739053.1:n.2553T>G
XR_001739054.1:n.2475T>G
XR_001739055.2:n.2492T>G
XR_001739056.2:n.2477T>G
XR_001739057.1:n.2493T>G
XR_001739058.1:n.2672T>G
XR_001739059.2:n.2405T>G
XR_001739060.1:n.2379T>G
XR_001739061.1:n.2421T>G
XR_001739062.1:n.2598T>G
XR_001739063.1:n.2305T>G
XR_001739064.1:n.2566T>G
XR_001739065.1:n.2510T>G
XR_001739066.1:n.2307T>G
XR_001739067.1:n.2214T>G
XR_001739068.1:n.2235T>G
XR_001739069.1:n.2412T>G
XR_001739070.1:n.2276T>G
XR_001739071.1:n.2134T>G
XR_001739072.1:n.2380T>G
XR_001739073.2:n.1591+3721T>G
XR_002959364.1:n.2306T>G
NM_001137550.2:c.1459+3721T>G MANE Select	NP_001131022.1:n.1459+3721T>G
NM_001137552.2:c.2213T>G	NP_001131024.1:p.Ile738Ser
NM_001137553.2:c.2045T>G	NP_001131025.1:p.Ile682Ser
NM_004735.4:c.2141T>G	NP_004726.2:p.Ile714Ser
NM_001137551.2:c.721+3721T>G	NP_001131023.1:n.721+3721T>G