Canonical Allele Identifier: CA2514454993

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99337004del , CM000666.2:g.99337004del GRCh38
NC_000004.11:g.100258161del , CM000666.1:g.100258161del GRCh37
NC_000004.10:g.100477184del NCBI36
NG_011718.1:g.20757del

Transcript Alleles

HGVS Amino-acid change
ENST00000515683.6:c.1104-228del (ADH1C) MANE Select ENSP00000426083.1:n.1104-228del
ENST00000639454.1:c.18+15654del (ADH1B) ENSP00000491622.1:n.18+15654del
ENST00000515683.5:c.1104-228del (ADH1C) ENSP00000426083.1:n.1104-228del
NM_000669.4:c.1104-228del (ADH1C) NP_000660.1:n.1104-228del
NR_133005.1:n.1430-228del (ADH1C)
XM_011531588.1:c.1002-228del (ADH1C) XP_011529890.1:n.1002-228del
XM_011531589.1:c.984-228del (ADH1C) XP_011529891.1:n.984-228del
NM_000669.5:c.1104-228del (ADH1C) MANE Select NP_000660.1:n.1104-228del
NR_133005.2:n.1131-228del (ADH1C)