Canonical Allele Identifier: CA645570111

Gene: TYR

Linked Data

• COSMIC: COSM5702426

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178537_89178538delinsTT , CM000673.2:g.89178537_89178538delinsTT	GRCh38
NC_000011.9:g.88911705_88911706delinsTT , CM000673.1:g.88911705_88911706delinsTT	GRCh37
NC_000011.8:g.88551353_88551354delinsTT	NCBI36
NG_008748.1:g.5666_5667delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.584_585delinsTT MANE Select	ENSP00000263321.4:p.Trp195Phe
ENST00000263321.5:c.584_585delinsTT	ENSP00000263321.4:p.Trp195Phe
ENST00000526139.1:n.645_646delinsTT
NM_000372.4:c.584_585delinsTT	NP_000363.1:p.Trp195Phe
XM_011542970.1:c.584_585delinsTT	XP_011541272.1:p.Trp195Phe
XM_011542970.2:c.584_585delinsTT	XP_011541272.1:p.Trp195Phe
XR_001748321.1:n.2718-65005_2718-65004delinsAA
XR_001748322.1:n.2733-65005_2733-65004delinsAA
NM_000372.5:c.584_585delinsTT MANE Select	NP_000363.1:p.Trp195Phe