Canonical Allele Identifier: CA1989920700

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178507_89178508delinsTG , CM000673.2:g.89178507_89178508delinsTG	GRCh38
NC_000011.9:g.88911675_88911676delinsTG , CM000673.1:g.88911675_88911676delinsTG	GRCh37
NC_000011.8:g.88551323_88551324delinsTG	NCBI36
NG_008748.1:g.5636_5637delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.554_555delinsTG MANE Select	ENSP00000263321.4:p.Met185=
ENST00000263321.5:c.554_555delinsTG	ENSP00000263321.4:p.Met185=
ENST00000526139.1:n.615_616delinsTG
NM_000372.4:c.554_555delinsTG	NP_000363.1:p.Met185=
XM_011542970.1:c.554_555delinsTG	XP_011541272.1:p.Met185=
XM_011542970.2:c.554_555delinsTG	XP_011541272.1:p.Met185=
XR_001748321.1:n.2718-64975_2718-64974delinsCA
XR_001748322.1:n.2733-64975_2733-64974delinsCA
NM_000372.5:c.554_555delinsTG MANE Select	NP_000363.1:p.Met185=