Canonical Allele Identifier: CA2552381425

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99337063_99337064insGTACTGGAAGCTCCACGACAAAAAGAAAATGCTGGTGGCAAGGCTCAAAGGCTATCTGGACGGTTTGCCCCCGAAGACACGCAGGCGCATCGTGCTGGCGATGCTCGCCGCCTTTGCGGTGCTTGCCCT , CM000666.2:g.99337063_99337064insGTACTGGAAGCTCCACGACAAAAAGAAAATGCTGGTGGCAAGGCTCAAAGGCTATCTGGACGGTTTGCCCCCGAAGACACGCAGGCGCATCGTGCTGGCGATGCTCGCCGCCTTTGCGGTGCTTGCCCT GRCh38
NC_000004.11:g.100258220_100258221insGTACTGGAAGCTCCACGACAAAAAGAAAATGCTGGTGGCAAGGCTCAAAGGCTATCTGGACGGTTTGCCCCCGAAGACACGCAGGCGCATCGTGCTGGCGATGCTCGCCGCCTTTGCGGTGCTTGCCCT , CM000666.1:g.100258220_100258221insGTACTGGAAGCTCCACGACAAAAAGAAAATGCTGGTGGCAAGGCTCAAAGGCTATCTGGACGGTTTGCCCCCGAAGACACGCAGGCGCATCGTGCTGGCGATGCTCGCCGCCTTTGCGGTGCTTGCCCT GRCh37
NC_000004.10:g.100477243_100477244insGTACTGGAAGCTCCACGACAAAAAGAAAATGCTGGTGGCAAGGCTCAAAGGCTATCTGGACGGTTTGCCCCCGAAGACACGCAGGCGCATCGTGCTGGCGATGCTCGCCGCCTTTGCGGTGCTTGCCCT NCBI36
NG_011718.1:g.20697_20698insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000515683.6:c.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C) MANE Select ENSP00000426083.1:n.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCG...
ENST00000639454.1:c.18+15594_18+15595insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1B) ENSP00000491622.1:n.18+15594_18+15595insAGGGCAAGCACCGCAAAGGCG...
ENST00000515683.5:c.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C) ENSP00000426083.1:n.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCG...
NM_000669.4:c.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C) NP_000660.1:n.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCGGCGAGC...
NR_133005.1:n.1430-288_1430-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C)
XM_011531588.1:c.1002-288_1002-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C) XP_011529890.1:n.1002-288_1002-287insAGGGCAAGCACCGCAAAGGCGGCG...
XM_011531589.1:c.984-288_984-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C) XP_011529891.1:n.984-288_984-287insAGGGCAAGCACCGCAAAGGCGGCGAG...
NM_000669.5:c.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C) MANE Select NP_000660.1:n.1104-288_1104-287insAGGGCAAGCACCGCAAAGGCGGCGAGC...
NR_133005.2:n.1131-288_1131-287insAGGGCAAGCACCGCAAAGGCGGCGAGCATCGCCAGCACGATGCGCCTGCGTGTCTTCGGGGGCAAACCGTCCAGATAGCCTTTGAGCCTTGCCACCAGCATTTTCTTTTTGTCGTGGAGCTTCCAGTAC (ADH1C)