Canonical Allele Identifier: CA1989972193

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284932C= , CM000673.2:g.89284932C=	GRCh38
NC_000011.9:g.89018100C= , CM000673.1:g.89018100C=	GRCh37
NC_000011.8:g.88657748C=	NCBI36
NG_008748.1:g.112061C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1344C= MANE Select	ENSP00000263321.4:p.Asp448=
ENST00000263321.5:c.1344C=	ENSP00000263321.4:p.Asp448=
ENST00000528243.1:n.342C=
NM_000372.4:c.1344C=	NP_000363.1:p.Asp448=
XM_011542970.1:c.1344C=	XP_011541272.1:p.Asp448=
XM_011542970.2:c.1344C=	XP_011541272.1:p.Asp448=
XR_001748321.1:n.2456+1102G=
XR_001748322.1:n.2457+1102G=
NM_000372.5:c.1344C= MANE Select	NP_000363.1:p.Asp448=