Canonical Allele Identifier: CA1989920074

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178333G= , CM000673.2:g.89178333G=	GRCh38
NC_000011.9:g.88911501G= , CM000673.1:g.88911501G=	GRCh37
NC_000011.8:g.88551149G=	NCBI36
NG_008748.1:g.5462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.380G= MANE Select	ENSP00000263321.4:p.Ser127=
ENST00000263321.5:c.380G=	ENSP00000263321.4:p.Ser127=
ENST00000526139.1:n.441G=
NM_000372.4:c.380G=	NP_000363.1:p.Ser127=
XM_011542970.1:c.380G=	XP_011541272.1:p.Ser127=
XM_011542970.2:c.380G=	XP_011541272.1:p.Ser127=
XR_001748321.1:n.2718-64800C=
XR_001748322.1:n.2733-64800C=
NM_000372.5:c.380G= MANE Select	NP_000363.1:p.Ser127=