Canonical Allele Identifier: CA1989919726
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178228_89178229delinsCT , CM000673.2:g.89178228_89178229delinsCT GRCh38
NC_000011.9:g.88911396_88911397delinsCT , CM000673.1:g.88911396_88911397delinsCT GRCh37
NC_000011.8:g.88551044_88551045delinsCT NCBI36
NG_008748.1:g.5357_5358delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.275_276delinsCT MANE Select ENSP00000263321.4:p.Ser92=
ENST00000263321.5:c.275_276delinsCT ENSP00000263321.4:p.Ser92=
ENST00000526139.1:n.336_337delinsCT
NM_000372.4:c.275_276delinsCT NP_000363.1:p.Ser92=
XM_011542970.1:c.275_276delinsCT XP_011541272.1:p.Ser92=
XM_011542970.2:c.275_276delinsCT XP_011541272.1:p.Ser92=
XR_001748321.1:n.2718-64696_2718-64695delinsAG
XR_001748322.1:n.2733-64696_2733-64695delinsAG
NM_000372.5:c.275_276delinsCT MANE Select NP_000363.1:p.Ser92=
Search 100 bp 5'
Search 100 bp 3'