Canonical Allele Identifier: CA2671506508

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124326-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124326T>G , CM000666.2:g.99124326T>G	GRCh38
NC_000004.11:g.100045477T>G , CM000666.1:g.100045477T>G	GRCh37
NC_000004.10:g.100264500T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.*116A>C MANE Select	ENSP00000265512.7:n.*116A>C
ENST00000265512.11:c.*116A>C	ENSP00000265512.7:n.*116A>C
ENST00000508393.5:c.*116A>C	ENSP00000424630.1:n.*116A>C
ENST00000629236.2:c.*80A>C	ENSP00000486450.1:n.*80A>C
NM_000670.3:c.*116A>C	NP_000661.2:n.*116A>C
NM_000670.4:c.*116A>C	NP_000661.2:n.*116A>C
NM_001306171.1:c.*116A>C	NP_001293100.1:n.*116A>C
NM_001306172.1:c.*116A>C	NP_001293101.1:n.*116A>C
NR_037884.1:n.429-9229T>G
XR_938685.1:n.1598A>C
XR_938686.1:n.1589A>C
XR_938687.1:n.1462A>C
NM_000670.5:c.*116A>C MANE Select	NP_000661.2:n.*116A>C
NM_001306171.2:c.*116A>C	NP_001293100.1:n.*116A>C
NM_001306172.2:c.*116A>C	NP_001293101.1:n.*116A>C