Canonical Allele Identifier: CA681530788

Gene: TYR

Linked Data

• dbSNP Id: rs941386065
• gnomAD v3: 11-89285211-G-GA
• gnomAD v4: 11-89285211-G-GA
• MyVariant Identifiers: chr11:g.89018379_89018380insA (hg19) ; chr11:g.89285211_89285212insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89285220dup , CM000673.2:g.89285220dup	GRCh38
NC_000011.9:g.89018388dup , CM000673.1:g.89018388dup	GRCh37
NC_000011.8:g.88658036dup	NCBI36
NG_008748.1:g.112349dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.1366+266dup MANE Select	ENSP00000263321.4:n.1366+266dup
ENST00000263321.5:c.1366+266dup	ENSP00000263321.4:n.1366+266dup
ENST00000528243.1:n.364+266dup
NM_000372.4:c.1366+266dup	NP_000363.1:n.1366+266dup
XM_011542970.1:c.1366+266dup	XP_011541272.1:n.1366+266dup
XM_011542970.2:c.1366+266dup	XP_011541272.1:n.1366+266dup
XR_001748321.1:n.2456+822dup
XR_001748322.1:n.2457+822dup
NM_000372.5:c.1366+266dup MANE Select	NP_000363.1:n.1366+266dup