Canonical Allele Identifier: CA2671506608

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124398-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124398G>A , CM000666.2:g.99124398G>A	GRCh38
NC_000004.11:g.100045549G>A , CM000666.1:g.100045549G>A	GRCh37
NC_000004.10:g.100264572G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*44C>T MANE Select	ENSP00000265512.7:n.*44C>T
ENST00000265512.11:c.*44C>T	ENSP00000265512.7:n.*44C>T
ENST00000505590.5:c.*44C>T	ENSP00000425416.1:n.*44C>T
ENST00000508393.5:c.*44C>T	ENSP00000424630.1:n.*44C>T
ENST00000509471.5:c.541C>T	ENSP00000424583.1:n.541C>T
ENST00000629236.2:c.*8C>T	ENSP00000486450.1:n.*8C>T
NM_000670.3:c.*44C>T	NP_000661.2:n.*44C>T
NM_000670.4:c.*44C>T	NP_000661.2:n.*44C>T
NM_001306171.1:c.*44C>T	NP_001293100.1:n.*44C>T
NM_001306172.1:c.*44C>T	NP_001293101.1:n.*44C>T
NR_037884.1:n.429-9157G>A
XR_938685.1:n.1526C>T
XR_938686.1:n.1517C>T
XR_938687.1:n.1390C>T
NM_000670.5:c.*44C>T MANE Select	NP_000661.2:n.*44C>T
NM_001306171.2:c.*44C>T	NP_001293100.1:n.*44C>T
NM_001306172.2:c.*44C>T	NP_001293101.1:n.*44C>T