Canonical Allele Identifier: CA1655112499

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873141T= , CM000668.2:g.111873141T=	GRCh38
NC_000006.11:g.112194344T= , CM000668.1:g.112194344T=	GRCh37
NC_000006.10:g.112301037T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-296A=	ENSP00000357671.3:n.-296A=
ENST00000354650.7:c.-296A= MANE Select	ENSP00000346671.3:n.-296A=
ENST00000368678.8:c.-226A=	ENSP00000357667.4:n.-226A=
ENST00000484067.6:c.-296A=	ENSP00000428983.1:n.-296A=
ENST00000518295.5:c.-413A=	ENSP00000428695.1:n.-413A=
ENST00000523238.5:c.-255A=	ENSP00000430364.1:n.-255A=
NM_002037.5:c.-296A= MANE Select	NP_002028.1:n.-296A=
XM_005266890.2:c.-296A=	XP_005266947.1:n.-296A=
XM_005266892.2:c.-296A=	XP_005266949.1:n.-296A=
XM_011535662.1:c.-296A=	XP_011533964.1:n.-296A=
XM_011535663.1:c.-255A=	XP_011533965.1:n.-255A=
XM_011536304.1:c.410T=	XP_011534606.1:p.Leu137=
XM_024446614.1:c.410T=	XP_024302382.1:p.Leu137=