Canonical Allele Identifier: CA1989921098

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178630_89178633delinsCAGG , CM000673.2:g.89178630_89178633delinsCAGG	GRCh38
NC_000011.9:g.88911798_88911801delinsCAGG , CM000673.1:g.88911798_88911801delinsCAGG	GRCh37
NC_000011.8:g.88551446_88551449delinsCAGG	NCBI36
NG_008748.1:g.5759_5762delinsCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.677_680delinsCAGG MANE Select	ENSP00000263321.4:p.Thr226=
ENST00000263321.5:c.677_680delinsCAGG	ENSP00000263321.4:p.Thr226=
ENST00000526139.1:n.738_741delinsCAGG
NM_000372.4:c.677_680delinsCAGG	NP_000363.1:p.Thr226=
XM_011542970.1:c.677_680delinsCAGG	XP_011541272.1:p.Thr226=
XM_011542970.2:c.677_680delinsCAGG	XP_011541272.1:p.Thr226=
XR_001748321.1:n.2718-65100_2718-65097delinsCCTG
XR_001748322.1:n.2733-65100_2733-65097delinsCCTG
NM_000372.5:c.677_680delinsCAGG MANE Select	NP_000363.1:p.Thr226=