Canonical Allele Identifier: CA2830782728
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178214_89178221delinsTTATTAA , CM000673.2:g.89178214_89178221delinsTTATTAA GRCh38
NC_000011.9:g.88911382_88911389delinsTTATTAA , CM000673.1:g.88911382_88911389delinsTTATTAA GRCh37
NC_000011.8:g.88551030_88551037delinsTTATTAA NCBI36
NG_008748.1:g.5343_5350delinsTTATTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.261_268delinsTTATTAA MANE Select ENSP00000263321.4:p.Arg87SerfsTer3
ENST00000263321.5:c.261_268delinsTTATTAA ENSP00000263321.4:p.Arg87SerfsTer3
ENST00000526139.1:n.322_329delinsTTATTAA
NM_000372.4:c.261_268delinsTTATTAA NP_000363.1:p.Arg87SerfsTer3
XM_011542970.1:c.261_268delinsTTATTAA XP_011541272.1:p.Arg87SerfsTer3
XM_011542970.2:c.261_268delinsTTATTAA XP_011541272.1:p.Arg87SerfsTer3
XR_001748321.1:n.2718-64688_2718-64681delinsTTAATAA
XR_001748322.1:n.2733-64688_2733-64681delinsTTAATAA
NM_000372.5:c.261_268delinsTTATTAA MANE Select NP_000363.1:p.Arg87SerfsTer3
Search 100 bp 5'
Search 100 bp 3'