Canonical Allele Identifier: CA1655112510

Gene: FYN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.111873152G= , CM000668.2:g.111873152G=	GRCh38
NC_000006.11:g.112194355G= , CM000668.1:g.112194355G=	GRCh37
NC_000006.10:g.112301048G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368682.8:c.-307C=	ENSP00000357671.3:n.-307C=
ENST00000354650.7:c.-307C= MANE Select	ENSP00000346671.3:n.-307C=
ENST00000368678.8:c.-237C=	ENSP00000357667.4:n.-237C=
ENST00000484067.6:c.-307C=	ENSP00000428983.1:n.-307C=
ENST00000518295.5:c.-424C=	ENSP00000428695.1:n.-424C=
ENST00000523238.5:c.-266C=	ENSP00000430364.1:n.-266C=
NM_002037.5:c.-307C= MANE Select	NP_002028.1:n.-307C=
XM_005266890.2:c.-307C=	XP_005266947.1:n.-307C=
XM_005266892.2:c.-307C=	XP_005266949.1:n.-307C=
XM_011535662.1:c.-307C=	XP_011533964.1:n.-307C=
XM_011535663.1:c.-266C=	XP_011533965.1:n.-266C=
XM_011536304.1:c.421G=	XP_011534606.1:p.Ala141=
XM_024446614.1:c.421G=	XP_024302382.1:p.Ala141=