Canonical Allele Identifier: CA2671506515
Gene: ADH4 HGNC NCBI

Linked Data

gnomAD v4: 4-99124330-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124330T>A , CM000666.2:g.99124330T>A GRCh38
NC_000004.11:g.100045481T>A , CM000666.1:g.100045481T>A GRCh37
NC_000004.10:g.100264504T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.*112A>T MANE Select ENSP00000265512.7:n.*112A>T
ENST00000265512.11:c.*112A>T ENSP00000265512.7:n.*112A>T
ENST00000508393.5:c.*112A>T ENSP00000424630.1:n.*112A>T
ENST00000629236.2:c.*76A>T ENSP00000486450.1:n.*76A>T
NM_000670.3:c.*112A>T NP_000661.2:n.*112A>T
NM_000670.4:c.*112A>T NP_000661.2:n.*112A>T
NM_001306171.1:c.*112A>T NP_001293100.1:n.*112A>T
NM_001306172.1:c.*112A>T NP_001293101.1:n.*112A>T
NR_037884.1:n.429-9225T>A
XR_938685.1:n.1594A>T
XR_938686.1:n.1585A>T
XR_938687.1:n.1458A>T
NM_000670.5:c.*112A>T MANE Select NP_000661.2:n.*112A>T
NM_001306171.2:c.*112A>T NP_001293100.1:n.*112A>T
NM_001306172.2:c.*112A>T NP_001293101.1:n.*112A>T