Canonical Allele Identifier: CA1655112565

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873240C= , CM000668.2:g.111873240C=	GRCh38
NC_000006.11:g.112194443C= , CM000668.1:g.112194443C=	GRCh37
NC_000006.10:g.112301136C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-395G=	ENSP00000357671.3:n.-395G=
ENST00000354650.7:c.-395G= MANE Select	ENSP00000346671.3:n.-395G=
ENST00000368678.8:c.-325G=	ENSP00000357667.4:n.-325G=
ENST00000484067.6:c.-361+30G=	ENSP00000428983.1:n.-361+30G=
ENST00000518295.5:c.-512G=	ENSP00000428695.1:n.-512G=
ENST00000523238.5:c.-354G=	ENSP00000430364.1:n.-354G=
NM_002037.5:c.-395G= MANE Select	NP_002028.1:n.-395G=
XM_005266890.2:c.-395G=	XP_005266947.1:n.-395G=
XM_005266892.2:c.-395G=	XP_005266949.1:n.-395G=
XM_011535662.1:c.-395G=	XP_011533964.1:n.-395G=
XM_011535663.1:c.-354G=	XP_011533965.1:n.-354G=
XM_011536304.1:c.509C=	XP_011534606.1:p.Ala170=
XM_024446614.1:c.509C=	XP_024302382.1:p.Ala170=