Canonical Allele Identifier: CA1479859412
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124349T= , CM000666.2:g.99124349T= GRCh38
NC_000004.11:g.100045500T= , CM000666.1:g.100045500T= GRCh37
NC_000004.10:g.100264523T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.*93A= MANE Select ENSP00000265512.7:n.*93A=
ENST00000265512.11:c.*93A= ENSP00000265512.7:n.*93A=
ENST00000508393.5:c.*93A= ENSP00000424630.1:n.*93A=
ENST00000629236.2:c.*57A= ENSP00000486450.1:n.*57A=
NM_000670.3:c.*93A= NP_000661.2:n.*93A=
NM_000670.4:c.*93A= NP_000661.2:n.*93A=
NM_001306171.1:c.*93A= NP_001293100.1:n.*93A=
NM_001306172.1:c.*93A= NP_001293101.1:n.*93A=
NR_037884.1:n.429-9206T=
XR_938685.1:n.1575A=
XR_938686.1:n.1566A=
XR_938687.1:n.1439A=
NM_000670.5:c.*93A= MANE Select NP_000661.2:n.*93A=
NM_001306171.2:c.*93A= NP_001293100.1:n.*93A=
NM_001306172.2:c.*93A= NP_001293101.1:n.*93A=