Canonical Allele Identifier: CA1989972202

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284935T= , CM000673.2:g.89284935T=	GRCh38
NC_000011.9:g.89018103T= , CM000673.1:g.89018103T=	GRCh37
NC_000011.8:g.88657751T=	NCBI36
NG_008748.1:g.112064T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1347T= MANE Select	ENSP00000263321.4:p.Tyr449=
ENST00000263321.5:c.1347T=	ENSP00000263321.4:p.Tyr449=
ENST00000528243.1:n.345T=
NM_000372.4:c.1347T=	NP_000363.1:p.Tyr449=
XM_011542970.1:c.1347T=	XP_011541272.1:p.Tyr449=
XM_011542970.2:c.1347T=	XP_011541272.1:p.Tyr449=
XR_001748321.1:n.2456+1099A=
XR_001748322.1:n.2457+1099A=
NM_000372.5:c.1347T= MANE Select	NP_000363.1:p.Tyr449=