Canonical Allele Identifier: CA382035477
Gene: TYR HGNC NCBI

Linked Data

COSMIC: COSM545765

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178735A>C , CM000673.2:g.89178735A>C GRCh38
NC_000011.9:g.88911903A>C , CM000673.1:g.88911903A>C GRCh37
NC_000011.8:g.88551551A>C NCBI36
NG_008748.1:g.5864A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.782A>C MANE Select ENSP00000263321.4:p.Asn261Thr
ENST00000263321.5:c.782A>C ENSP00000263321.4:p.Asn261Thr
ENST00000526139.1:n.843A>C
NM_000372.4:c.782A>C NP_000363.1:p.Asn261Thr
XM_011542970.1:c.782A>C XP_011541272.1:p.Asn261Thr
XM_011542970.2:c.782A>C XP_011541272.1:p.Asn261Thr
XR_001748321.1:n.2718-65202T>G
XR_001748322.1:n.2733-65202T>G
NM_000372.5:c.782A>C MANE Select NP_000363.1:p.Asn261Thr