Canonical Allele Identifier: CA2680044059

Gene: FYN

Linked Data

• gnomAD v4: 6-111873149-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873149G>T , CM000668.2:g.111873149G>T	GRCh38
NC_000006.11:g.112194352G>T , CM000668.1:g.112194352G>T	GRCh37
NC_000006.10:g.112301045G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-304C>A	ENSP00000357671.3:n.-304C>A
ENST00000354650.7:c.-304C>A MANE Select	ENSP00000346671.3:n.-304C>A
ENST00000368678.8:c.-234C>A	ENSP00000357667.4:n.-234C>A
ENST00000484067.6:c.-304C>A	ENSP00000428983.1:n.-304C>A
ENST00000518295.5:c.-421C>A	ENSP00000428695.1:n.-421C>A
ENST00000523238.5:c.-263C>A	ENSP00000430364.1:n.-263C>A
NM_002037.5:c.-304C>A MANE Select	NP_002028.1:n.-304C>A
XM_005266890.2:c.-304C>A	XP_005266947.1:n.-304C>A
XM_005266892.2:c.-304C>A	XP_005266949.1:n.-304C>A
XM_011535662.1:c.-304C>A	XP_011533964.1:n.-304C>A
XM_011535663.1:c.-263C>A	XP_011533965.1:n.-263C>A
XM_011536304.1:c.418G>T	XP_011534606.1:p.Ala140Ser
XM_024446614.1:c.418G>T	XP_024302382.1:p.Ala140Ser