Canonical Allele Identifier: CA1065910128

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99337000_99337002del , CM000666.2:g.99337000_99337002del GRCh38
NC_000004.11:g.100258157_100258159del , CM000666.1:g.100258157_100258159del GRCh37
NC_000004.10:g.100477180_100477182del NCBI36
NG_011718.1:g.20759_20761del

Transcript Alleles

HGVS Amino-acid change
ENST00000515683.6:c.1104-226_1104-224del (ADH1C) MANE Select ENSP00000426083.1:n.1104-226_1104-224del
ENST00000639454.1:c.18+15656_18+15658del (ADH1B) ENSP00000491622.1:n.18+15656_18+15658del
ENST00000515683.5:c.1104-226_1104-224del (ADH1C) ENSP00000426083.1:n.1104-226_1104-224del
NM_000669.4:c.1104-226_1104-224del (ADH1C) NP_000660.1:n.1104-226_1104-224del
NR_133005.1:n.1430-226_1430-224del (ADH1C)
XM_011531588.1:c.1002-226_1002-224del (ADH1C) XP_011529890.1:n.1002-226_1002-224del
XM_011531589.1:c.984-226_984-224del (ADH1C) XP_011529891.1:n.984-226_984-224del
NM_000669.5:c.1104-226_1104-224del (ADH1C) MANE Select NP_000660.1:n.1104-226_1104-224del
NR_133005.2:n.1131-226_1131-224del (ADH1C)