Canonical Allele Identifier: CA2671506528
Gene: ADH4 HGNC NCBI

Linked Data

gnomAD v4: 4-99124334-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124334A>T , CM000666.2:g.99124334A>T GRCh38
NC_000004.11:g.100045485A>T , CM000666.1:g.100045485A>T GRCh37
NC_000004.10:g.100264508A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.*108T>A MANE Select ENSP00000265512.7:n.*108T>A
ENST00000265512.11:c.*108T>A ENSP00000265512.7:n.*108T>A
ENST00000508393.5:c.*108T>A ENSP00000424630.1:n.*108T>A
ENST00000629236.2:c.*72T>A ENSP00000486450.1:n.*72T>A
NM_000670.3:c.*108T>A NP_000661.2:n.*108T>A
NM_000670.4:c.*108T>A NP_000661.2:n.*108T>A
NM_001306171.1:c.*108T>A NP_001293100.1:n.*108T>A
NM_001306172.1:c.*108T>A NP_001293101.1:n.*108T>A
NR_037884.1:n.429-9221A>T
XR_938685.1:n.1590T>A
XR_938686.1:n.1581T>A
XR_938687.1:n.1454T>A
NM_000670.5:c.*108T>A MANE Select NP_000661.2:n.*108T>A
NM_001306171.2:c.*108T>A NP_001293100.1:n.*108T>A
NM_001306172.2:c.*108T>A NP_001293101.1:n.*108T>A
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