Canonical Allele Identifier: CA2671506602

Gene: ADH4

Linked Data

• gnomAD v4: 4-99124395-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124395C>G , CM000666.2:g.99124395C>G	GRCh38
NC_000004.11:g.100045546C>G , CM000666.1:g.100045546C>G	GRCh37
NC_000004.10:g.100264569C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.*47G>C MANE Select	ENSP00000265512.7:n.*47G>C
ENST00000265512.11:c.*47G>C	ENSP00000265512.7:n.*47G>C
ENST00000505590.5:c.*47G>C	ENSP00000425416.1:n.*47G>C
ENST00000508393.5:c.*47G>C	ENSP00000424630.1:n.*47G>C
ENST00000509471.5:c.544G>C	ENSP00000424583.1:n.544G>C
ENST00000629236.2:c.*11G>C	ENSP00000486450.1:n.*11G>C
NM_000670.3:c.*47G>C	NP_000661.2:n.*47G>C
NM_000670.4:c.*47G>C	NP_000661.2:n.*47G>C
NM_001306171.1:c.*47G>C	NP_001293100.1:n.*47G>C
NM_001306172.1:c.*47G>C	NP_001293101.1:n.*47G>C
NR_037884.1:n.429-9160C>G
XR_938685.1:n.1529G>C
XR_938686.1:n.1520G>C
XR_938687.1:n.1393G>C
NM_000670.5:c.*47G>C MANE Select	NP_000661.2:n.*47G>C
NM_001306171.2:c.*47G>C	NP_001293100.1:n.*47G>C
NM_001306172.2:c.*47G>C	NP_001293101.1:n.*47G>C