Canonical Allele Identifier: CA1479867815
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99144295C= , CM000666.2:g.99144295C= GRCh38
NC_000004.11:g.100065446C= , CM000666.1:g.100065446C= GRCh37
NC_000004.10:g.100284469C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.-73G= MANE Select ENSP00000265512.7:n.-73G=
ENST00000265512.11:c.-73G= ENSP00000265512.7:n.-73G=
ENST00000504581.1:n.170-1515G=
ENST00000504894.1:c.-134G= ENSP00000427261.1:n.-134G=
ENST00000508393.5:c.-164G= ENSP00000424630.1:n.-164G=
NM_000670.3:c.-73G= NP_000661.2:n.-73G=
NM_000670.4:c.-73G= NP_000661.2:n.-73G=
NM_001306171.1:c.-164G= NP_001293100.1:n.-164G=
NM_001306172.1:c.-156G= NP_001293101.1:n.-156G=
NR_037884.1:n.680-10250C=
XR_938685.1:n.16G=
XR_938687.1:n.20G=
NM_000670.5:c.-73G= MANE Select NP_000661.2:n.-73G=
NM_001306171.2:c.-164G= NP_001293100.1:n.-164G=
NM_001306172.2:c.-156G= NP_001293101.1:n.-156G=