Canonical Allele Identifier: CA1479962111

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99340923G= , CM000666.2:g.99340923G= GRCh38
NC_000004.11:g.100262080G= , CM000666.1:g.100262080G= GRCh37
NC_000004.10:g.100481103G= NCBI36
NG_011718.1:g.16838C=

Transcript Alleles

HGVS Amino-acid change
ENST00000515683.6:c.829-213C= (ADH1C) MANE Select ENSP00000426083.1:n.829-213C=
ENST00000639454.1:c.18+11735C= (ADH1B) ENSP00000491622.1:n.18+11735C=
ENST00000515683.5:c.829-213C= (ADH1C) ENSP00000426083.1:n.829-213C=
NM_000669.4:c.829-213C= (ADH1C) NP_000660.1:n.829-213C=
NR_133005.1:n.1155-213C= (ADH1C)
XM_011531588.1:c.727-213C= (ADH1C) XP_011529890.1:n.727-213C=
XM_011531589.1:c.709-213C= (ADH1C) XP_011529891.1:n.709-213C=
NM_000669.5:c.829-213C= (ADH1C) MANE Select NP_000660.1:n.829-213C=
NR_133005.2:n.856-213C= (ADH1C)