Canonical Allele Identifier: CA2695215156
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178409del , CM000673.2:g.89178409del GRCh38
NC_000011.9:g.88911577del , CM000673.1:g.88911577del GRCh37
NC_000011.8:g.88551225del NCBI36
NG_008748.1:g.5538del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.456del MANE Select ENSP00000263321.4:p.Ile153Ter
ENST00000263321.5:c.456del ENSP00000263321.4:p.Ile153Ter
ENST00000526139.1:n.517del
NM_000372.4:c.456del NP_000363.1:p.Ile153Ter
XM_011542970.1:c.456del XP_011541272.1:p.Ile153Ter
XM_011542970.2:c.456del XP_011541272.1:p.Ile153Ter
XR_001748321.1:n.2718-64873del
XR_001748322.1:n.2733-64873del
NM_000372.5:c.456del MANE Select NP_000363.1:p.Ile153Ter
Search 100 bp 5'
Search 100 bp 3'