Canonical Allele Identifier: CA1989920907

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178571_89178579delinsTTTTCTGCC , CM000673.2:g.89178571_89178579delinsTTTTCTGCC	GRCh38
NC_000011.9:g.88911739_88911747delinsTTTTCTGCC , CM000673.1:g.88911739_88911747delinsTTTTCTGCC	GRCh37
NC_000011.8:g.88551387_88551395delinsTTTTCTGCC	NCBI36
NG_008748.1:g.5700_5708delinsTTTTCTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.618_626delinsTTTTCTGCC MANE Select	ENSP00000263321.4:p.Ala206=
ENST00000263321.5:c.618_626delinsTTTTCTGCC	ENSP00000263321.4:p.Ala206=
ENST00000526139.1:n.679_687delinsTTTTCTGCC
NM_000372.4:c.618_626delinsTTTTCTGCC	NP_000363.1:p.Ala206=
XM_011542970.1:c.618_626delinsTTTTCTGCC	XP_011541272.1:p.Ala206=
XM_011542970.2:c.618_626delinsTTTTCTGCC	XP_011541272.1:p.Ala206=
XR_001748321.1:n.2718-65046_2718-65038delinsGGCAGAAAA
XR_001748322.1:n.2733-65046_2733-65038delinsGGCAGAAAA
NM_000372.5:c.618_626delinsTTTTCTGCC MANE Select	NP_000363.1:p.Ala206=