Canonical Allele Identifier: CA1479859444
Gene: ADH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124433C= , CM000666.2:g.99124433C= GRCh38
NC_000004.11:g.100045584C= , CM000666.1:g.100045584C= GRCh37
NC_000004.10:g.100264607C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.*9G= MANE Select ENSP00000265512.7:n.*9G=
ENST00000265512.11:c.*9G= ENSP00000265512.7:n.*9G=
ENST00000505590.5:c.*9G= ENSP00000425416.1:n.*9G=
ENST00000508393.5:c.*9G= ENSP00000424630.1:n.*9G=
ENST00000509471.5:c.506G= ENSP00000424583.1:n.506G=
ENST00000629236.2:c.1149G= ENSP00000486450.1:p.Gln383=
NM_000670.3:c.*9G= NP_000661.2:n.*9G=
NM_000670.4:c.*9G= NP_000661.2:n.*9G=
NM_001306171.1:c.*9G= NP_001293100.1:n.*9G=
NM_001306172.1:c.*9G= NP_001293101.1:n.*9G=
NR_037884.1:n.429-9122C=
XR_938685.1:n.1491G=
XR_938686.1:n.1482G=
XR_938687.1:n.1355G=
NM_000670.5:c.*9G= MANE Select NP_000661.2:n.*9G=
NM_001306171.2:c.*9G= NP_001293100.1:n.*9G=
NM_001306172.2:c.*9G= NP_001293101.1:n.*9G=