Canonical Allele Identifier: CA1989919865
Gene: TYR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178272_89178286delinsTTTTGGGGACCAAAC , CM000673.2:g.89178272_89178286delinsTTTTGGGGACCAAAC GRCh38
NC_000011.9:g.88911440_88911454delinsTTTTGGGGACCAAAC , CM000673.1:g.88911440_88911454delinsTTTTGGGGACCAAAC GRCh37
NC_000011.8:g.88551088_88551102delinsTTTTGGGGACCAAAC NCBI36
NG_008748.1:g.5401_5415delinsTTTTGGGGACCAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.319_333delinsTTTTGGGGACCAAAC MANE Select ENSP00000263321.4:p.Phe107=
ENST00000263321.5:c.319_333delinsTTTTGGGGACCAAAC ENSP00000263321.4:p.Phe107=
ENST00000526139.1:n.380_394delinsTTTTGGGGACCAAAC
NM_000372.4:c.319_333delinsTTTTGGGGACCAAAC NP_000363.1:p.Phe107=
XM_011542970.1:c.319_333delinsTTTTGGGGACCAAAC XP_011541272.1:p.Phe107=
XM_011542970.2:c.319_333delinsTTTTGGGGACCAAAC XP_011541272.1:p.Phe107=
XR_001748321.1:n.2718-64753_2718-64739delinsGTTTGGTCCCCAAAA
XR_001748322.1:n.2733-64753_2733-64739delinsGTTTGGTCCCCAAAA
NM_000372.5:c.319_333delinsTTTTGGGGACCAAAC MANE Select NP_000363.1:p.Phe107=
Search 100 bp 5'
Search 100 bp 3'