Canonical Allele Identifier: CA2671506512
Gene: ADH4 HGNC NCBI

Linked Data

gnomAD v4: 4-99124328-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124328A>C , CM000666.2:g.99124328A>C GRCh38
NC_000004.11:g.100045479A>C , CM000666.1:g.100045479A>C GRCh37
NC_000004.10:g.100264502A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000265512.12:c.*114T>G MANE Select ENSP00000265512.7:n.*114T>G
ENST00000265512.11:c.*114T>G ENSP00000265512.7:n.*114T>G
ENST00000508393.5:c.*114T>G ENSP00000424630.1:n.*114T>G
ENST00000629236.2:c.*78T>G ENSP00000486450.1:n.*78T>G
NM_000670.3:c.*114T>G NP_000661.2:n.*114T>G
NM_000670.4:c.*114T>G NP_000661.2:n.*114T>G
NM_001306171.1:c.*114T>G NP_001293100.1:n.*114T>G
NM_001306172.1:c.*114T>G NP_001293101.1:n.*114T>G
NR_037884.1:n.429-9227A>C
XR_938685.1:n.1596T>G
XR_938686.1:n.1587T>G
XR_938687.1:n.1460T>G
NM_000670.5:c.*114T>G MANE Select NP_000661.2:n.*114T>G
NM_001306171.2:c.*114T>G NP_001293100.1:n.*114T>G
NM_001306172.2:c.*114T>G NP_001293101.1:n.*114T>G