Canonical Allele Identifier: CA2793086053

Gene: TYR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285021_89285022insC , CM000673.2:g.89285021_89285022insC	GRCh38
NC_000011.9:g.89018189_89018190insC , CM000673.1:g.89018189_89018190insC	GRCh37
NC_000011.8:g.88657837_88657838insC	NCBI36
NG_008748.1:g.112150_112151insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+67_1366+68insC MANE Select	ENSP00000263321.4:n.1366+67_1366+68insC
ENST00000263321.5:c.1366+67_1366+68insC	ENSP00000263321.4:n.1366+67_1366+68insC
ENST00000528243.1:n.364+67_364+68insC
NM_000372.4:c.1366+67_1366+68insC	NP_000363.1:n.1366+67_1366+68insC
XM_011542970.1:c.1366+67_1366+68insC	XP_011541272.1:n.1366+67_1366+68insC
XM_011542970.2:c.1366+67_1366+68insC	XP_011541272.1:n.1366+67_1366+68insC
XR_001748321.1:n.2456+1012_2456+1013insG
XR_001748322.1:n.2457+1012_2457+1013insG
NM_000372.5:c.1366+67_1366+68insC MANE Select	NP_000363.1:n.1366+67_1366+68insC