Canonical Allele Identifier: CA1479859415
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124354G= , CM000666.2:g.99124354G= GRCh38
NC_000004.11:g.100045505G= , CM000666.1:g.100045505G= GRCh37
NC_000004.10:g.100264528G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.*88C= MANE Select ENSP00000265512.7:n.*88C=
ENST00000265512.11:c.*88C= ENSP00000265512.7:n.*88C=
ENST00000508393.5:c.*88C= ENSP00000424630.1:n.*88C=
ENST00000629236.2:c.*52C= ENSP00000486450.1:n.*52C=
NM_000670.3:c.*88C= NP_000661.2:n.*88C=
NM_000670.4:c.*88C= NP_000661.2:n.*88C=
NM_001306171.1:c.*88C= NP_001293100.1:n.*88C=
NM_001306172.1:c.*88C= NP_001293101.1:n.*88C=
NR_037884.1:n.429-9201G=
XR_938685.1:n.1570C=
XR_938686.1:n.1561C=
XR_938687.1:n.1434C=
NM_000670.5:c.*88C= MANE Select NP_000661.2:n.*88C=
NM_001306171.2:c.*88C= NP_001293100.1:n.*88C=
NM_001306172.2:c.*88C= NP_001293101.1:n.*88C=