Canonical Allele Identifier: CA1655112571

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873255C= , CM000668.2:g.111873255C=	GRCh38
NC_000006.11:g.112194458C= , CM000668.1:g.112194458C=	GRCh37
NC_000006.10:g.112301151C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-410G=	ENSP00000357671.3:n.-410G=
ENST00000354650.7:c.-410G= MANE Select	ENSP00000346671.3:n.-410G=
ENST00000368678.8:c.-340G=	ENSP00000357667.4:n.-340G=
ENST00000484067.6:c.-361+15G=	ENSP00000428983.1:n.-361+15G=
ENST00000518295.5:c.-527G=	ENSP00000428695.1:n.-527G=
ENST00000523238.5:c.-369G=	ENSP00000430364.1:n.-369G=
NM_002037.5:c.-410G= MANE Select	NP_002028.1:n.-410G=
XM_005266890.2:c.-410G=	XP_005266947.1:n.-410G=
XM_005266892.2:c.-410G=	XP_005266949.1:n.-410G=
XM_011535662.1:c.-410G=	XP_011533964.1:n.-410G=
XM_011535663.1:c.-369G=	XP_011533965.1:n.-369G=
XM_011536304.1:c.524C=	XP_011534606.1:p.Pro175=
XM_024446614.1:c.524C=	XP_024302382.1:p.Pro175=