Canonical Allele Identifier: CA1989920621

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178482G= , CM000673.2:g.89178482G=	GRCh38
NC_000011.9:g.88911650G= , CM000673.1:g.88911650G=	GRCh37
NC_000011.8:g.88551298G=	NCBI36
NG_008748.1:g.5611G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.529G= MANE Select	ENSP00000263321.4:p.Val177=
ENST00000263321.5:c.529G=	ENSP00000263321.4:p.Val177=
ENST00000526139.1:n.590G=
NM_000372.4:c.529G=	NP_000363.1:p.Val177=
XM_011542970.1:c.529G=	XP_011541272.1:p.Val177=
XM_011542970.2:c.529G=	XP_011541272.1:p.Val177=
XR_001748321.1:n.2718-64949C=
XR_001748322.1:n.2733-64949C=
NM_000372.5:c.529G= MANE Select	NP_000363.1:p.Val177=