Canonical Allele Identifier: CA2695215170
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178660_89178661insAG , CM000673.2:g.89178660_89178661insAG GRCh38
NC_000011.9:g.88911828_88911829insAG , CM000673.1:g.88911828_88911829insAG GRCh37
NC_000011.8:g.88551476_88551477insAG NCBI36
NG_008748.1:g.5789_5790insAG

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.707_708insAG MANE Select ENSP00000263321.4:p.Trp236Ter
ENST00000263321.5:c.707_708insAG ENSP00000263321.4:p.Trp236Ter
ENST00000526139.1:n.768_769insAG
NM_000372.4:c.707_708insAG NP_000363.1:p.Trp236Ter
XM_011542970.1:c.707_708insAG XP_011541272.1:p.Trp236Ter
XM_011542970.2:c.707_708insAG XP_011541272.1:p.Trp236Ter
XR_001748321.1:n.2718-65127_2718-65126insTC
XR_001748322.1:n.2733-65127_2733-65126insTC
NM_000372.5:c.707_708insAG MANE Select NP_000363.1:p.Trp236Ter
Search 100 bp 5'
Search 100 bp 3'