Canonical Allele Identifier: CA645570105
Gene: TYR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178358dup , CM000673.2:g.89178358dup GRCh38
NC_000011.9:g.88911526dup , CM000673.1:g.88911526dup GRCh37
NC_000011.8:g.88551174dup NCBI36
NG_008748.1:g.5487dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.405dup MANE Select ENSP00000263321.4:p.Ala136CysfsTer?
ENST00000263321.5:c.405dup ENSP00000263321.4:p.Ala136CysfsTer?
ENST00000526139.1:n.466dup
NM_000372.4:c.405dup NP_000363.1:p.Ala136CysfsTer?
XM_011542970.1:c.405dup XP_011541272.1:p.Ala136CysfsTer?
XM_011542970.2:c.405dup XP_011541272.1:p.Ala136CysfsTer?
XR_001748321.1:n.2718-64820dup
XR_001748322.1:n.2733-64820dup
NM_000372.5:c.405dup MANE Select NP_000363.1:p.Ala136CysfsTer?