Canonical Allele Identifier: CA476321101

Gene: TYR

Linked Data

• MyVariant Identifiers: chr11:g.89018110C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89284942C>T , CM000673.2:g.89284942C>T	GRCh38
NC_000011.9:g.89018110C>T , CM000673.1:g.89018110C>T	GRCh37
NC_000011.8:g.88657758C>T	NCBI36
NG_008748.1:g.112071C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1354C>T MANE Select	ENSP00000263321.4:p.Leu452=
ENST00000263321.5:c.1354C>T	ENSP00000263321.4:p.Leu452=
ENST00000528243.1:n.352C>T
NM_000372.4:c.1354C>T	NP_000363.1:p.Leu452=
XM_011542970.1:c.1354C>T	XP_011541272.1:p.Leu452=
XM_011542970.2:c.1354C>T	XP_011541272.1:p.Leu452=
XR_001748321.1:n.2456+1092G>A
XR_001748322.1:n.2457+1092G>A
NM_000372.5:c.1354C>T MANE Select	NP_000363.1:p.Leu452=