Canonical Allele Identifier: CA2671506521
Gene: ADH4 HGNC NCBI

Linked Data

gnomAD v4: 4-99124332-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124332T>C , CM000666.2:g.99124332T>C GRCh38
NC_000004.11:g.100045483T>C , CM000666.1:g.100045483T>C GRCh37
NC_000004.10:g.100264506T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.*110A>G MANE Select ENSP00000265512.7:n.*110A>G
ENST00000265512.11:c.*110A>G ENSP00000265512.7:n.*110A>G
ENST00000508393.5:c.*110A>G ENSP00000424630.1:n.*110A>G
ENST00000629236.2:c.*74A>G ENSP00000486450.1:n.*74A>G
NM_000670.3:c.*110A>G NP_000661.2:n.*110A>G
NM_000670.4:c.*110A>G NP_000661.2:n.*110A>G
NM_001306171.1:c.*110A>G NP_001293100.1:n.*110A>G
NM_001306172.1:c.*110A>G NP_001293101.1:n.*110A>G
NR_037884.1:n.429-9223T>C
XR_938685.1:n.1592A>G
XR_938686.1:n.1583A>G
XR_938687.1:n.1456A>G
NM_000670.5:c.*110A>G MANE Select NP_000661.2:n.*110A>G
NM_001306171.2:c.*110A>G NP_001293100.1:n.*110A>G
NM_001306172.2:c.*110A>G NP_001293101.1:n.*110A>G