Canonical Allele Identifier: CA2671506969

Gene: ADH4

Linked Data

• gnomAD v4: 4-99126884-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126884C>G , CM000666.2:g.99126884C>G	GRCh38
NC_000004.11:g.100048035C>G , CM000666.1:g.100048035C>G	GRCh37
NC_000004.10:g.100267058C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.980-152G>C MANE Select	ENSP00000265512.7:n.980-152G>C
ENST00000265512.11:c.980-152G>C	ENSP00000265512.7:n.980-152G>C
ENST00000505590.5:c.1037-152G>C	ENSP00000425416.1:n.1037-152G>C
ENST00000506705.5:c.*954-152G>C	ENSP00000426667.1:n.*954-152G>C
ENST00000508393.5:c.1037-152G>C	ENSP00000424630.1:n.1037-152G>C
ENST00000509471.5:c.334-152G>C	ENSP00000424583.1:n.334-152G>C
ENST00000629236.2:c.980-152G>C	ENSP00000486450.1:n.980-152G>C
NM_000670.3:c.980-152G>C	NP_000661.2:n.980-152G>C
NM_000670.4:c.980-152G>C	NP_000661.2:n.980-152G>C
NM_001306171.1:c.1037-152G>C	NP_001293100.1:n.1037-152G>C
NM_001306172.1:c.1037-152G>C	NP_001293101.1:n.1037-152G>C
NR_037884.1:n.429-6671C>G
XR_938685.1:n.1208-152G>C
XR_938686.1:n.1199-152G>C
XR_938687.1:n.1072-152G>C
NM_000670.5:c.980-152G>C MANE Select	NP_000661.2:n.980-152G>C
NM_001306171.2:c.1037-152G>C	NP_001293100.1:n.1037-152G>C
NM_001306172.2:c.1037-152G>C	NP_001293101.1:n.1037-152G>C