Canonical Allele Identifier: CA1941454113

Gene: ARMS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122455720_122455733delinsTTGAACCCCTTCCC , CM000672.2:g.122455720_122455733delinsTTGAACCCCTTCCC	GRCh38
NC_000010.10:g.124215236_124215249delinsTTGAACCCCTTCCC , CM000672.1:g.124215236_124215249delinsTTGAACCCCTTCCC	GRCh37
NC_000010.9:g.124205226_124205239delinsTTGAACCCCTTCCC	NCBI36
NG_011725.1:g.6058_6071delinsTTGAACCCCTTCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000528446.1:c.297+696_297+709delinsTTGAACCCCTTCCC MANE Select	ENSP00000436682.1:n.297+696_297+709delinsTTGAACCCCTTCCC
NM_001099667.1:c.297+696_297+709delinsTTGAACCCCTTCCC	NP_001093137.1:n.297+696_297+709delinsTTGAACCCCTTCCC
XR_946382.1:n.1827+2762_1827+2775delinsGGGAAGGGGTTCAA
XR_946383.1:n.1827+2762_1827+2775delinsGGGAAGGGGTTCAA
XR_946384.1:n.1576+2762_1576+2775delinsGGGAAGGGGTTCAA
XR_946385.1:n.1828-712_1828-699delinsGGGAAGGGGTTCAA
NM_001099667.2:c.297+696_297+709delinsTTGAACCCCTTCCC	NP_001093137.1:n.297+696_297+709delinsTTGAACCCCTTCCC
XR_946382.2:n.1855+2762_1855+2775delinsGGGAAGGGGTTCAA
XR_946383.2:n.1855+2762_1855+2775delinsGGGAAGGGGTTCAA
XR_946384.2:n.1580+2762_1580+2775delinsGGGAAGGGGTTCAA
XR_946385.2:n.1856-712_1856-699delinsGGGAAGGGGTTCAA
NM_001099667.3:c.297+696_297+709delinsTTGAACCCCTTCCC MANE Select	NP_001093137.1:n.297+696_297+709delinsTTGAACCCCTTCCC