Canonical Allele Identifier: CA1093201883

Gene: FYN

Linked Data

• gnomAD v3: 6-111873242-G-A
• gnomAD v4: 6-111873242-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873242G>A , CM000668.2:g.111873242G>A	GRCh38
NC_000006.11:g.112194445G>A , CM000668.1:g.112194445G>A	GRCh37
NC_000006.10:g.112301138G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-397C>T	ENSP00000357671.3:n.-397C>T
ENST00000354650.7:c.-397C>T MANE Select	ENSP00000346671.3:n.-397C>T
ENST00000368678.8:c.-327C>T	ENSP00000357667.4:n.-327C>T
ENST00000484067.6:c.-361+28C>T	ENSP00000428983.1:n.-361+28C>T
ENST00000518295.5:c.-514C>T	ENSP00000428695.1:n.-514C>T
ENST00000523238.5:c.-356C>T	ENSP00000430364.1:n.-356C>T
NM_002037.5:c.-397C>T MANE Select	NP_002028.1:n.-397C>T
XM_005266890.2:c.-397C>T	XP_005266947.1:n.-397C>T
XM_005266892.2:c.-397C>T	XP_005266949.1:n.-397C>T
XM_011535662.1:c.-397C>T	XP_011533964.1:n.-397C>T
XM_011535663.1:c.-356C>T	XP_011533965.1:n.-356C>T
XM_011536304.1:c.511G>A	XP_011534606.1:p.Gly171Arg
XM_024446614.1:c.511G>A	XP_024302382.1:p.Gly171Arg