Canonical Allele Identifier: CA1989920796

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178535C= , CM000673.2:g.89178535C=	GRCh38
NC_000011.9:g.88911703C= , CM000673.1:g.88911703C=	GRCh37
NC_000011.8:g.88551351C=	NCBI36
NG_008748.1:g.5664C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.582C= MANE Select	ENSP00000263321.4:p.Ile194=
ENST00000263321.5:c.582C=	ENSP00000263321.4:p.Ile194=
ENST00000526139.1:n.643C=
NM_000372.4:c.582C=	NP_000363.1:p.Ile194=
XM_011542970.1:c.582C=	XP_011541272.1:p.Ile194=
XM_011542970.2:c.582C=	XP_011541272.1:p.Ile194=
XR_001748321.1:n.2718-65002G=
XR_001748322.1:n.2733-65002G=
NM_000372.5:c.582C= MANE Select	NP_000363.1:p.Ile194=