Canonical Allele Identifier: CA382078187

Gene: TYR

Linked Data

• MyVariant Identifiers: chr11:g.89018118T>A (hg19) ; chr11:g.89284950T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284950T>A , CM000673.2:g.89284950T>A	GRCh38
NC_000011.9:g.89018118T>A , CM000673.1:g.89018118T>A	GRCh37
NC_000011.8:g.88657766T>A	NCBI36
NG_008748.1:g.112079T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1362T>A MANE Select	ENSP00000263321.4:p.Asp454Glu
ENST00000263321.5:c.1362T>A	ENSP00000263321.4:p.Asp454Glu
ENST00000528243.1:n.360T>A
NM_000372.4:c.1362T>A	NP_000363.1:p.Asp454Glu
XM_011542970.1:c.1362T>A	XP_011541272.1:p.Asp454Glu
XM_011542970.2:c.1362T>A	XP_011541272.1:p.Asp454Glu
XR_001748321.1:n.2456+1084A>T
XR_001748322.1:n.2457+1084A>T
NM_000372.5:c.1362T>A MANE Select	NP_000363.1:p.Asp454Glu