Canonical Allele Identifier: CA214412173

Gene: ARMS2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122456869_122456870insA , CM000672.2:g.122456869_122456870insA	GRCh38
NC_000010.10:g.124216385_124216386insA , CM000672.1:g.124216385_124216386insA	GRCh37
NC_000010.9:g.124206375_124206376insA	NCBI36
NG_011554.1:g.345_346insA
NG_011725.1:g.7207_7208insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528446.1:c.298-38_298-37insA MANE Select	ENSP00000436682.1:n.298-38_298-37insA
NM_001099667.1:c.298-38_298-37insA	NP_001093137.1:n.298-38_298-37insA
XR_946382.1:n.1827+1625_1827+1626insT
XR_946383.1:n.1827+1625_1827+1626insT
XR_946384.1:n.1576+1625_1576+1626insT
XR_946385.1:n.1827+1625_1827+1626insT
NM_001099667.2:c.298-38_298-37insA	NP_001093137.1:n.298-38_298-37insA
XR_946382.2:n.1855+1625_1855+1626insT
XR_946383.2:n.1855+1625_1855+1626insT
XR_946384.2:n.1580+1625_1580+1626insT
XR_946385.2:n.1855+1625_1855+1626insT
NM_001099667.3:c.298-38_298-37insA MANE Select	NP_001093137.1:n.298-38_298-37insA