Canonical Allele Identifier: CA1989920931

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178584_89178586delinsCAT , CM000673.2:g.89178584_89178586delinsCAT	GRCh38
NC_000011.9:g.88911752_88911754delinsCAT , CM000673.1:g.88911752_88911754delinsCAT	GRCh37
NC_000011.8:g.88551400_88551402delinsCAT	NCBI36
NG_008748.1:g.5713_5715delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.631_633delinsCAT MANE Select	ENSP00000263321.4:p.His211=
ENST00000263321.5:c.631_633delinsCAT	ENSP00000263321.4:p.His211=
ENST00000526139.1:n.692_694delinsCAT
NM_000372.4:c.631_633delinsCAT	NP_000363.1:p.His211=
XM_011542970.1:c.631_633delinsCAT	XP_011541272.1:p.His211=
XM_011542970.2:c.631_633delinsCAT	XP_011541272.1:p.His211=
XR_001748321.1:n.2718-65053_2718-65051delinsATG
XR_001748322.1:n.2733-65053_2733-65051delinsATG
NM_000372.5:c.631_633delinsCAT MANE Select	NP_000363.1:p.His211=