Canonical Allele Identifier: CA1989921134

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178645_89178646delinsTC , CM000673.2:g.89178645_89178646delinsTC	GRCh38
NC_000011.9:g.88911813_88911814delinsTC , CM000673.1:g.88911813_88911814delinsTC	GRCh37
NC_000011.8:g.88551461_88551462delinsTC	NCBI36
NG_008748.1:g.5774_5775delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.692_693delinsTC MANE Select	ENSP00000263321.4:p.Phe231=
ENST00000263321.5:c.692_693delinsTC	ENSP00000263321.4:p.Phe231=
ENST00000526139.1:n.753_754delinsTC
NM_000372.4:c.692_693delinsTC	NP_000363.1:p.Phe231=
XM_011542970.1:c.692_693delinsTC	XP_011541272.1:p.Phe231=
XM_011542970.2:c.692_693delinsTC	XP_011541272.1:p.Phe231=
XR_001748321.1:n.2718-65113_2718-65112delinsGA
XR_001748322.1:n.2733-65113_2733-65112delinsGA
NM_000372.5:c.692_693delinsTC MANE Select	NP_000363.1:p.Phe231=