Canonical Allele Identifier: CA1479960130

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99336918_99336923delinsGGTCAA , CM000666.2:g.99336918_99336923delinsGGTCAA GRCh38
NC_000004.11:g.100258075_100258080delinsGGTCAA , CM000666.1:g.100258075_100258080delinsGGTCAA GRCh37
NC_000004.10:g.100477098_100477103delinsGGTCAA NCBI36
NG_011718.1:g.20838_20843delinsTTGACC

Transcript Alleles

HGVS Amino-acid change
ENST00000515683.6:c.1104-147_1104-142delinsTTGACC (ADH1C) MANE Select ENSP00000426083.1:n.1104-147_1104-142delinsTTGACC
ENST00000639454.1:c.18+15735_18+15740delinsTTGACC (ADH1B) ENSP00000491622.1:n.18+15735_18+15740delinsTTGACC
ENST00000515683.5:c.1104-147_1104-142delinsTTGACC (ADH1C) ENSP00000426083.1:n.1104-147_1104-142delinsTTGACC
NM_000669.4:c.1104-147_1104-142delinsTTGACC (ADH1C) NP_000660.1:n.1104-147_1104-142delinsTTGACC
NR_133005.1:n.1430-147_1430-142delinsTTGACC (ADH1C)
XM_011531588.1:c.1002-147_1002-142delinsTTGACC (ADH1C) XP_011529890.1:n.1002-147_1002-142delinsTTGACC
XM_011531589.1:c.984-147_984-142delinsTTGACC (ADH1C) XP_011529891.1:n.984-147_984-142delinsTTGACC
NM_000669.5:c.1104-147_1104-142delinsTTGACC (ADH1C) MANE Select NP_000660.1:n.1104-147_1104-142delinsTTGACC
NR_133005.2:n.1131-147_1131-142delinsTTGACC (ADH1C)