Canonical Allele Identifier: CA1989972605

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285130_89285131delinsTC , CM000673.2:g.89285130_89285131delinsTC	GRCh38
NC_000011.9:g.89018298_89018299delinsTC , CM000673.1:g.89018298_89018299delinsTC	GRCh37
NC_000011.8:g.88657946_88657947delinsTC	NCBI36
NG_008748.1:g.112259_112260delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+176_1366+177delinsTC MANE Select	ENSP00000263321.4:n.1366+176_1366+177delinsTC
ENST00000263321.5:c.1366+176_1366+177delinsTC	ENSP00000263321.4:n.1366+176_1366+177delinsTC
ENST00000528243.1:n.364+176_364+177delinsTC
NM_000372.4:c.1366+176_1366+177delinsTC	NP_000363.1:n.1366+176_1366+177delinsTC
XM_011542970.1:c.1366+176_1366+177delinsTC	XP_011541272.1:n.1366+176_1366+177delinsTC
XM_011542970.2:c.1366+176_1366+177delinsTC	XP_011541272.1:n.1366+176_1366+177delinsTC
XR_001748321.1:n.2456+903_2456+904delinsGA
XR_001748322.1:n.2457+903_2457+904delinsGA
NM_000372.5:c.1366+176_1366+177delinsTC MANE Select	NP_000363.1:n.1366+176_1366+177delinsTC