Canonical Allele Identifier: CA1989971774

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284807C= , CM000673.2:g.89284807C=	GRCh38
NC_000011.9:g.89017975C= , CM000673.1:g.89017975C=	GRCh37
NC_000011.8:g.88657623C=	NCBI36
NG_008748.1:g.111936C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263321.6:c.1219C= MANE Select	ENSP00000263321.4:p.Leu407=
ENST00000263321.5:c.1219C=	ENSP00000263321.4:p.Leu407=
ENST00000528243.1:n.217C=
NM_000372.4:c.1219C=	NP_000363.1:p.Leu407=
XM_011542970.1:c.1219C=	XP_011541272.1:p.Leu407=
XM_011542970.2:c.1219C=	XP_011541272.1:p.Leu407=
XR_001748321.1:n.2456+1227G=
XR_001748322.1:n.2457+1227G=
NM_000372.5:c.1219C= MANE Select	NP_000363.1:p.Leu407=