Canonical Allele Identifier: CA1989921141
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178648_89178649delinsCT , CM000673.2:g.89178648_89178649delinsCT GRCh38
NC_000011.9:g.88911816_88911817delinsCT , CM000673.1:g.88911816_88911817delinsCT GRCh37
NC_000011.8:g.88551464_88551465delinsCT NCBI36
NG_008748.1:g.5777_5778delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.695_696delinsCT MANE Select ENSP00000263321.4:p.Thr232=
ENST00000263321.5:c.695_696delinsCT ENSP00000263321.4:p.Thr232=
ENST00000526139.1:n.756_757delinsCT
NM_000372.4:c.695_696delinsCT NP_000363.1:p.Thr232=
XM_011542970.1:c.695_696delinsCT XP_011541272.1:p.Thr232=
XM_011542970.2:c.695_696delinsCT XP_011541272.1:p.Thr232=
XR_001748321.1:n.2718-65116_2718-65115delinsAG
XR_001748322.1:n.2733-65116_2733-65115delinsAG
NM_000372.5:c.695_696delinsCT MANE Select NP_000363.1:p.Thr232=
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