Canonical Allele Identifier: CA1065910140

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99337021_99337022del , CM000666.2:g.99337021_99337022del GRCh38
NC_000004.11:g.100258178_100258179del , CM000666.1:g.100258178_100258179del GRCh37
NC_000004.10:g.100477201_100477202del NCBI36
NG_011718.1:g.20739_20740del

Transcript Alleles

HGVS Amino-acid change
ENST00000515683.6:c.1104-246_1104-245del (ADH1C) MANE Select ENSP00000426083.1:n.1104-246_1104-245del
ENST00000639454.1:c.18+15636_18+15637del (ADH1B) ENSP00000491622.1:n.18+15636_18+15637del
ENST00000515683.5:c.1104-246_1104-245del (ADH1C) ENSP00000426083.1:n.1104-246_1104-245del
NM_000669.4:c.1104-246_1104-245del (ADH1C) NP_000660.1:n.1104-246_1104-245del
NR_133005.1:n.1430-246_1430-245del (ADH1C)
XM_011531588.1:c.1002-246_1002-245del (ADH1C) XP_011529890.1:n.1002-246_1002-245del
XM_011531589.1:c.984-246_984-245del (ADH1C) XP_011529891.1:n.984-246_984-245del
NM_000669.5:c.1104-246_1104-245del (ADH1C) MANE Select NP_000660.1:n.1104-246_1104-245del
NR_133005.2:n.1131-246_1131-245del (ADH1C)