Canonical Allele Identifier: CA433379426

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759238A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717746A>G , CM000665.2:g.43717746A>G	GRCh38
NC_000003.11:g.43759238A>G , CM000665.1:g.43759238A>G	GRCh37
NC_000003.10:g.43734242A>G	NCBI36
NG_007090.3:g.31864A>G
NG_007090.5:g.31877A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-20A>G
ENST00000454293.2:c.726A>G	ENSP00000412014.2:p.Lys242=
ENST00000458276.7:c.774-697A>G	ENSP00000390849.3:n.774-697A>G
ENST00000463153.2:c.76A>G
ENST00000642351.1:c.726A>G	ENSP00000494478.1:p.Lys242=
ENST00000643140.1:c.*211A>G	ENSP00000495588.1:n.*211A>G
ENST00000643477.1:c.*310A>G	ENSP00000496220.1:n.*310A>G
ENST00000643500.1:c.*50A>G	ENSP00000494735.1:n.*50A>G
ENST00000643520.1:n.1015A>G
ENST00000644371.2:c.849A>G MANE Select	ENSP00000495778.1:p.Lys283=
ENST00000646378.1:c.*899A>G	ENSP00000495826.1:n.*899A>G
ENST00000646799.1:c.*248-697A>G	ENSP00000494829.1:n.*248-697A>G
ENST00000649763.1:c.849A>G	ENSP00000497701.1:p.Lys283=
ENST00000413300.1:c.270-20A>G	ENSP00000392159.1:n.270-20A>G
ENST00000458276.6:c.849A>G	ENSP00000390849.2:p.Lys283=
ENST00000463153.1:n.79A>G
NM_016006.4:c.849A>G	NP_057090.2:p.Lys283=
XM_011533779.1:c.726A>G	XP_011532081.1:p.Lys242=
XM_011533780.1:c.774-697A>G	XP_011532082.1:n.774-697A>G
XR_940447.1:n.794A>G
NM_001355186.1:c.849A>G	NP_001342115.1:p.Lys283=
NM_001365649.1:c.726A>G	NP_001352578.1:p.Lys242=
NM_001365650.1:c.774-697A>G	NP_001352579.1:n.774-697A>G
NM_016006.5:c.849A>G	NP_057090.2:p.Lys283=
NR_158560.1:n.860A>G
NM_001355186.2:c.849A>G	NP_001342115.1:p.Lys283=
NM_016006.6:c.849A>G MANE Select	NP_057090.2:p.Lys283=