Canonical Allele Identifier: CA1989920725

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178520_89178521delinsTG , CM000673.2:g.89178520_89178521delinsTG	GRCh38
NC_000011.9:g.88911688_88911689delinsTG , CM000673.1:g.88911688_88911689delinsTG	GRCh37
NC_000011.8:g.88551336_88551337delinsTG	NCBI36
NG_008748.1:g.5649_5650delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.567_568delinsTG MANE Select	ENSP00000263321.4:p.Leu189=
ENST00000263321.5:c.567_568delinsTG	ENSP00000263321.4:p.Leu189=
ENST00000526139.1:n.628_629delinsTG
NM_000372.4:c.567_568delinsTG	NP_000363.1:p.Leu189=
XM_011542970.1:c.567_568delinsTG	XP_011541272.1:p.Leu189=
XM_011542970.2:c.567_568delinsTG	XP_011541272.1:p.Leu189=
XR_001748321.1:n.2718-64988_2718-64987delinsCA
XR_001748322.1:n.2733-64988_2733-64987delinsCA
NM_000372.5:c.567_568delinsTG MANE Select	NP_000363.1:p.Leu189=