Canonical Allele Identifier: CA1989919951
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178291_89178293delinsCAG , CM000673.2:g.89178291_89178293delinsCAG GRCh38
NC_000011.9:g.88911459_88911461delinsCAG , CM000673.1:g.88911459_88911461delinsCAG GRCh37
NC_000011.8:g.88551107_88551109delinsCAG NCBI36
NG_008748.1:g.5420_5422delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.338_340delinsCAG MANE Select ENSP00000263321.4:p.Thr113=
ENST00000263321.5:c.338_340delinsCAG ENSP00000263321.4:p.Thr113=
ENST00000526139.1:n.399_401delinsCAG
NM_000372.4:c.338_340delinsCAG NP_000363.1:p.Thr113=
XM_011542970.1:c.338_340delinsCAG XP_011541272.1:p.Thr113=
XM_011542970.2:c.338_340delinsCAG XP_011541272.1:p.Thr113=
XR_001748321.1:n.2718-64760_2718-64758delinsCTG
XR_001748322.1:n.2733-64760_2733-64758delinsCTG
NM_000372.5:c.338_340delinsCAG MANE Select NP_000363.1:p.Thr113=
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