Canonical Allele Identifier: CA352347405

Gene: ABHD5

Linked Data

• gnomAD v4: 3-43717676-A-G
• MyVariant Identifiers: chr3:g.43759168A>G (hg19) ; chr3:g.43717676A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717676A>G , CM000665.2:g.43717676A>G	GRCh38
NC_000003.11:g.43759168A>G , CM000665.1:g.43759168A>G	GRCh37
NC_000003.10:g.43734172A>G	NCBI36
NG_007090.3:g.31794A>G
NG_007090.5:g.31807A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-90A>G
ENST00000454293.2:c.656A>G	ENSP00000412014.2:p.Glu219Gly
ENST00000458276.7:c.774-767A>G	ENSP00000390849.3:n.774-767A>G
ENST00000463153.2:c.6A>G
ENST00000642351.1:c.656A>G	ENSP00000494478.1:p.Glu219Gly
ENST00000643140.1:c.*141A>G	ENSP00000495588.1:n.*141A>G
ENST00000643477.1:c.*240A>G	ENSP00000496220.1:n.*240A>G
ENST00000643500.1:c.667A>G	ENSP00000494735.1:p.Arg223Gly
ENST00000643520.1:n.945A>G
ENST00000644371.2:c.779A>G MANE Select	ENSP00000495778.1:p.Glu260Gly
ENST00000646378.1:c.*829A>G	ENSP00000495826.1:n.*829A>G
ENST00000646799.1:c.*248-767A>G	ENSP00000494829.1:n.*248-767A>G
ENST00000649763.1:c.779A>G	ENSP00000497701.1:p.Glu260Gly
ENST00000413300.1:c.270-90A>G	ENSP00000392159.1:n.270-90A>G
ENST00000458276.6:c.779A>G	ENSP00000390849.2:p.Glu260Gly
ENST00000463153.1:n.9A>G
NM_016006.4:c.779A>G	NP_057090.2:p.Glu260Gly
XM_011533779.1:c.656A>G	XP_011532081.1:p.Glu219Gly
XM_011533780.1:c.774-767A>G	XP_011532082.1:n.774-767A>G
XR_940447.1:n.724A>G
NM_001355186.1:c.779A>G	NP_001342115.1:p.Glu260Gly
NM_001365649.1:c.656A>G	NP_001352578.1:p.Glu219Gly
NM_001365650.1:c.774-767A>G	NP_001352579.1:n.774-767A>G
NM_016006.5:c.779A>G	NP_057090.2:p.Glu260Gly
NR_158560.1:n.790A>G
NM_001355186.2:c.779A>G	NP_001342115.1:p.Glu260Gly
NM_016006.6:c.779A>G MANE Select	NP_057090.2:p.Glu260Gly