Canonical Allele Identifier: CA1989920755

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178525_89178526delinsGA , CM000673.2:g.89178525_89178526delinsGA	GRCh38
NC_000011.9:g.88911693_88911694delinsGA , CM000673.1:g.88911693_88911694delinsGA	GRCh37
NC_000011.8:g.88551341_88551342delinsGA	NCBI36
NG_008748.1:g.5654_5655delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.572_573delinsGA MANE Select	ENSP00000263321.4:p.Gly191=
ENST00000263321.5:c.572_573delinsGA	ENSP00000263321.4:p.Gly191=
ENST00000526139.1:n.633_634delinsGA
NM_000372.4:c.572_573delinsGA	NP_000363.1:p.Gly191=
XM_011542970.1:c.572_573delinsGA	XP_011541272.1:p.Gly191=
XM_011542970.2:c.572_573delinsGA	XP_011541272.1:p.Gly191=
XR_001748321.1:n.2718-64993_2718-64992delinsTC
XR_001748322.1:n.2733-64993_2733-64992delinsTC
NM_000372.5:c.572_573delinsGA MANE Select	NP_000363.1:p.Gly191=