Canonical Allele Identifier: CA1655112567

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873247G= , CM000668.2:g.111873247G=	GRCh38
NC_000006.11:g.112194450G= , CM000668.1:g.112194450G=	GRCh37
NC_000006.10:g.112301143G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368682.8:c.-402C=	ENSP00000357671.3:n.-402C=
ENST00000354650.7:c.-402C= MANE Select	ENSP00000346671.3:n.-402C=
ENST00000368678.8:c.-332C=	ENSP00000357667.4:n.-332C=
ENST00000484067.6:c.-361+23C=	ENSP00000428983.1:n.-361+23C=
ENST00000518295.5:c.-519C=	ENSP00000428695.1:n.-519C=
ENST00000523238.5:c.-361C=	ENSP00000430364.1:n.-361C=
NM_002037.5:c.-402C= MANE Select	NP_002028.1:n.-402C=
XM_005266890.2:c.-402C=	XP_005266947.1:n.-402C=
XM_005266892.2:c.-402C=	XP_005266949.1:n.-402C=
XM_011535662.1:c.-402C=	XP_011533964.1:n.-402C=
XM_011535663.1:c.-361C=	XP_011533965.1:n.-361C=
XM_011536304.1:c.516G=	XP_011534606.1:p.Glu172=
XM_024446614.1:c.516G=	XP_024302382.1:p.Glu172=