Canonical Allele Identifier: CA1989919704
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178222_89178229delinsAGTGCTCT , CM000673.2:g.89178222_89178229delinsAGTGCTCT GRCh38
NC_000011.9:g.88911390_88911397delinsAGTGCTCT , CM000673.1:g.88911390_88911397delinsAGTGCTCT GRCh37
NC_000011.8:g.88551038_88551045delinsAGTGCTCT NCBI36
NG_008748.1:g.5351_5358delinsAGTGCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.269_276delinsAGTGCTCT MANE Select ENSP00000263321.4:p.Gln90=
ENST00000263321.5:c.269_276delinsAGTGCTCT ENSP00000263321.4:p.Gln90=
ENST00000526139.1:n.330_337delinsAGTGCTCT
NM_000372.4:c.269_276delinsAGTGCTCT NP_000363.1:p.Gln90=
XM_011542970.1:c.269_276delinsAGTGCTCT XP_011541272.1:p.Gln90=
XM_011542970.2:c.269_276delinsAGTGCTCT XP_011541272.1:p.Gln90=
XR_001748321.1:n.2718-64696_2718-64689delinsAGAGCACT
XR_001748322.1:n.2733-64696_2733-64689delinsAGAGCACT
NM_000372.5:c.269_276delinsAGTGCTCT MANE Select NP_000363.1:p.Gln90=
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