Canonical Allele Identifier: CA940690366

Gene: TYR

Linked Data

• dbSNP Id: rs1805218479
• gnomAD v3: 11-89285219-A-AT
• gnomAD v4: 11-89285219-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285219_89285220insT , CM000673.2:g.89285219_89285220insT	GRCh38
NC_000011.9:g.89018387_89018388insT , CM000673.1:g.89018387_89018388insT	GRCh37
NC_000011.8:g.88658035_88658036insT	NCBI36
NG_008748.1:g.112348_112349insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+265_1366+266insT MANE Select	ENSP00000263321.4:n.1366+265_1366+266insT
ENST00000263321.5:c.1366+265_1366+266insT	ENSP00000263321.4:n.1366+265_1366+266insT
ENST00000528243.1:n.364+265_364+266insT
NM_000372.4:c.1366+265_1366+266insT	NP_000363.1:n.1366+265_1366+266insT
XM_011542970.1:c.1366+265_1366+266insT	XP_011541272.1:n.1366+265_1366+266insT
XM_011542970.2:c.1366+265_1366+266insT	XP_011541272.1:n.1366+265_1366+266insT
XR_001748321.1:n.2456+814_2456+815insA
XR_001748322.1:n.2457+814_2457+815insA
NM_000372.5:c.1366+265_1366+266insT MANE Select	NP_000363.1:n.1366+265_1366+266insT