Canonical Allele Identifier: CA1479960132

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99336922A= , CM000666.2:g.99336922A= GRCh38
NC_000004.11:g.100258079A= , CM000666.1:g.100258079A= GRCh37
NC_000004.10:g.100477102A= NCBI36
NG_011718.1:g.20839T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000515683.6:c.1104-146T= (ADH1C) MANE Select ENSP00000426083.1:n.1104-146T=
ENST00000639454.1:c.18+15736T= (ADH1B) ENSP00000491622.1:n.18+15736T=
ENST00000515683.5:c.1104-146T= (ADH1C) ENSP00000426083.1:n.1104-146T=
NM_000669.4:c.1104-146T= (ADH1C) NP_000660.1:n.1104-146T=
NR_133005.1:n.1430-146T= (ADH1C)
XM_011531588.1:c.1002-146T= (ADH1C) XP_011529890.1:n.1002-146T=
XM_011531589.1:c.984-146T= (ADH1C) XP_011529891.1:n.984-146T=
NM_000669.5:c.1104-146T= (ADH1C) MANE Select NP_000660.1:n.1104-146T=
NR_133005.2:n.1131-146T= (ADH1C)