Canonical Allele Identifier: CA2680044056

Gene: FYN

Linked Data

• gnomAD v4: 6-111873138-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873138C>A , CM000668.2:g.111873138C>A	GRCh38
NC_000006.11:g.112194341C>A , CM000668.1:g.112194341C>A	GRCh37
NC_000006.10:g.112301034C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-293G>T	ENSP00000357671.3:n.-293G>T
ENST00000354650.7:c.-293G>T MANE Select	ENSP00000346671.3:n.-293G>T
ENST00000368678.8:c.-223G>T	ENSP00000357667.4:n.-223G>T
ENST00000484067.6:c.-293G>T	ENSP00000428983.1:n.-293G>T
ENST00000518295.5:c.-410G>T	ENSP00000428695.1:n.-410G>T
ENST00000523238.5:c.-252G>T	ENSP00000430364.1:n.-252G>T
NM_002037.5:c.-293G>T MANE Select	NP_002028.1:n.-293G>T
XM_005266890.2:c.-293G>T	XP_005266947.1:n.-293G>T
XM_005266892.2:c.-293G>T	XP_005266949.1:n.-293G>T
XM_011535662.1:c.-293G>T	XP_011533964.1:n.-293G>T
XM_011535663.1:c.-252G>T	XP_011533965.1:n.-252G>T
XM_011536304.1:c.407C>A	XP_011534606.1:p.Ser136Tyr
XM_024446614.1:c.407C>A	XP_024302382.1:p.Ser136Tyr