Canonical Allele Identifier: CA2671506551

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124353-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124353G>T , CM000666.2:g.99124353G>T	GRCh38
NC_000004.11:g.100045504G>T , CM000666.1:g.100045504G>T	GRCh37
NC_000004.10:g.100264527G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*89C>A MANE Select	ENSP00000265512.7:n.*89C>A
ENST00000265512.11:c.*89C>A	ENSP00000265512.7:n.*89C>A
ENST00000508393.5:c.*89C>A	ENSP00000424630.1:n.*89C>A
ENST00000629236.2:c.*53C>A	ENSP00000486450.1:n.*53C>A
NM_000670.3:c.*89C>A	NP_000661.2:n.*89C>A
NM_000670.4:c.*89C>A	NP_000661.2:n.*89C>A
NM_001306171.1:c.*89C>A	NP_001293100.1:n.*89C>A
NM_001306172.1:c.*89C>A	NP_001293101.1:n.*89C>A
NR_037884.1:n.429-9202G>T
XR_938685.1:n.1571C>A
XR_938686.1:n.1562C>A
XR_938687.1:n.1435C>A
NM_000670.5:c.*89C>A MANE Select	NP_000661.2:n.*89C>A
NM_001306171.2:c.*89C>A	NP_001293100.1:n.*89C>A
NM_001306172.2:c.*89C>A	NP_001293101.1:n.*89C>A