Canonical Allele Identifier: CA2680044062

Gene: FYN

Linked Data

• gnomAD v4: 6-111873153-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873153C>T , CM000668.2:g.111873153C>T	GRCh38
NC_000006.11:g.112194356C>T , CM000668.1:g.112194356C>T	GRCh37
NC_000006.10:g.112301049C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-308G>A	ENSP00000357671.3:n.-308G>A
ENST00000354650.7:c.-308G>A MANE Select	ENSP00000346671.3:n.-308G>A
ENST00000368678.8:c.-238G>A	ENSP00000357667.4:n.-238G>A
ENST00000484067.6:c.-308G>A	ENSP00000428983.1:n.-308G>A
ENST00000518295.5:c.-425G>A	ENSP00000428695.1:n.-425G>A
ENST00000523238.5:c.-267G>A	ENSP00000430364.1:n.-267G>A
NM_002037.5:c.-308G>A MANE Select	NP_002028.1:n.-308G>A
XM_005266890.2:c.-308G>A	XP_005266947.1:n.-308G>A
XM_005266892.2:c.-308G>A	XP_005266949.1:n.-308G>A
XM_011535662.1:c.-308G>A	XP_011533964.1:n.-308G>A
XM_011535663.1:c.-267G>A	XP_011533965.1:n.-267G>A
XM_011536304.1:c.422C>T	XP_011534606.1:p.Ala141Val
XM_024446614.1:c.422C>T	XP_024302382.1:p.Ala141Val