Canonical Allele Identifier: CA1655112494

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873132A= , CM000668.2:g.111873132A=	GRCh38
NC_000006.11:g.112194335A= , CM000668.1:g.112194335A=	GRCh37
NC_000006.10:g.112301028A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-287T=	ENSP00000357671.3:n.-287T=
ENST00000354650.7:c.-287T= MANE Select	ENSP00000346671.3:n.-287T=
ENST00000368678.8:c.-217T=	ENSP00000357667.4:n.-217T=
ENST00000484067.6:c.-287T=	ENSP00000428983.1:n.-287T=
ENST00000518295.5:c.-404T=	ENSP00000428695.1:n.-404T=
ENST00000523238.5:c.-246T=	ENSP00000430364.1:n.-246T=
NM_002037.5:c.-287T= MANE Select	NP_002028.1:n.-287T=
XM_005266890.2:c.-287T=	XP_005266947.1:n.-287T=
XM_005266892.2:c.-287T=	XP_005266949.1:n.-287T=
XM_011535662.1:c.-287T=	XP_011533964.1:n.-287T=
XM_011535663.1:c.-246T=	XP_011533965.1:n.-246T=
XM_011536304.1:c.401A=	XP_011534606.1:p.Asn134=
XM_024446614.1:c.401A=	XP_024302382.1:p.Asn134=