Canonical Allele Identifier: CA1989919877
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178275_89178277delinsTGG , CM000673.2:g.89178275_89178277delinsTGG GRCh38
NC_000011.9:g.88911443_88911445delinsTGG , CM000673.1:g.88911443_88911445delinsTGG GRCh37
NC_000011.8:g.88551091_88551093delinsTGG NCBI36
NG_008748.1:g.5404_5406delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.322_324delinsTGG MANE Select ENSP00000263321.4:p.Trp108=
ENST00000263321.5:c.322_324delinsTGG ENSP00000263321.4:p.Trp108=
ENST00000526139.1:n.383_385delinsTGG
NM_000372.4:c.322_324delinsTGG NP_000363.1:p.Trp108=
XM_011542970.1:c.322_324delinsTGG XP_011541272.1:p.Trp108=
XM_011542970.2:c.322_324delinsTGG XP_011541272.1:p.Trp108=
XR_001748321.1:n.2718-64744_2718-64742delinsCCA
XR_001748322.1:n.2733-64744_2733-64742delinsCCA
NM_000372.5:c.322_324delinsTGG MANE Select NP_000363.1:p.Trp108=
Search 100 bp 5'
Search 100 bp 3'