Canonical Allele Identifier: CA1655112495

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873136C= , CM000668.2:g.111873136C=	GRCh38
NC_000006.11:g.112194339C= , CM000668.1:g.112194339C=	GRCh37
NC_000006.10:g.112301032C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-291G=	ENSP00000357671.3:n.-291G=
ENST00000354650.7:c.-291G= MANE Select	ENSP00000346671.3:n.-291G=
ENST00000368678.8:c.-221G=	ENSP00000357667.4:n.-221G=
ENST00000484067.6:c.-291G=	ENSP00000428983.1:n.-291G=
ENST00000518295.5:c.-408G=	ENSP00000428695.1:n.-408G=
ENST00000523238.5:c.-250G=	ENSP00000430364.1:n.-250G=
NM_002037.5:c.-291G= MANE Select	NP_002028.1:n.-291G=
XM_005266890.2:c.-291G=	XP_005266947.1:n.-291G=
XM_005266892.2:c.-291G=	XP_005266949.1:n.-291G=
XM_011535662.1:c.-291G=	XP_011533964.1:n.-291G=
XM_011535663.1:c.-250G=	XP_011533965.1:n.-250G=
XM_011536304.1:c.405C=	XP_011534606.1:p.Pro135=
XM_024446614.1:c.405C=	XP_024302382.1:p.Pro135=