Canonical Allele Identifier: CA2793086086

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285063_89285064insACA , CM000673.2:g.89285063_89285064insACA	GRCh38
NC_000011.9:g.89018231_89018232insACA , CM000673.1:g.89018231_89018232insACA	GRCh37
NC_000011.8:g.88657879_88657880insACA	NCBI36
NG_008748.1:g.112192_112193insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+109_1366+110insACA MANE Select	ENSP00000263321.4:n.1366+109_1366+110insACA
ENST00000263321.5:c.1366+109_1366+110insACA	ENSP00000263321.4:n.1366+109_1366+110insACA
ENST00000528243.1:n.364+109_364+110insACA
NM_000372.4:c.1366+109_1366+110insACA	NP_000363.1:n.1366+109_1366+110insACA
XM_011542970.1:c.1366+109_1366+110insACA	XP_011541272.1:n.1366+109_1366+110insACA
XM_011542970.2:c.1366+109_1366+110insACA	XP_011541272.1:n.1366+109_1366+110insACA
XR_001748321.1:n.2456+970_2456+971insTGT
XR_001748322.1:n.2457+970_2457+971insTGT
NM_000372.5:c.1366+109_1366+110insACA MANE Select	NP_000363.1:n.1366+109_1366+110insACA