Canonical Allele Identifier: CA433377661

Gene: ABHD5

Linked Data

• COSMIC: COSM446529
• MyVariant Identifiers: chr3:g.43740768G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43699276G>A , CM000665.2:g.43699276G>A	GRCh38
NC_000003.11:g.43740768G>A , CM000665.1:g.43740768G>A	GRCh37
NC_000003.10:g.43715772G>A	NCBI36
NG_007090.3:g.13394G>A
NG_007090.5:g.13407G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013894.3:c.48G>A	ENSP00000013894.2:p.Arg16=
ENST00000454293.2:c.-76G>A	ENSP00000412014.2:n.-76G>A
ENST00000458276.7:c.48G>A	ENSP00000390849.3:p.Arg16=
ENST00000642351.1:c.-76G>A	ENSP00000494478.1:n.-76G>A
ENST00000643140.1:c.48G>A	ENSP00000495588.1:p.Arg16=
ENST00000643477.1:c.48G>A	ENSP00000496220.1:p.Arg16=
ENST00000643500.1:c.48G>A	ENSP00000494735.1:p.Arg16=
ENST00000643520.1:n.96G>A
ENST00000644371.2:c.48G>A MANE Select	ENSP00000495778.1:p.Arg16=
ENST00000646378.1:c.*98G>A	ENSP00000495826.1:n.*98G>A
ENST00000646799.1:c.48G>A	ENSP00000494829.1:p.Arg16=
ENST00000649763.1:c.48G>A	ENSP00000497701.1:p.Arg16=
ENST00000013894.2:c.48G>A	ENSP00000013894.2:p.Arg16=
ENST00000454293.1:c.-76G>A	ENSP00000412014.1:n.-76G>A
ENST00000456453.5:c.-76G>A	ENSP00000391582.1:n.-76G>A
ENST00000458276.6:c.48G>A	ENSP00000390849.2:p.Arg16=
ENST00000486764.1:n.149G>A
NM_016006.4:c.48G>A	NP_057090.2:p.Arg16=
XM_011533779.1:c.-76G>A	XP_011532081.1:n.-76G>A
XM_011533780.1:c.48G>A	XP_011532082.1:p.Arg16=
XR_940447.1:n.105G>A
NM_001355186.1:c.48G>A	NP_001342115.1:p.Arg16=
NM_001365649.1:c.-76G>A	NP_001352578.1:n.-76G>A
NM_001365650.1:c.48G>A	NP_001352579.1:p.Arg16=
NM_016006.5:c.48G>A	NP_057090.2:p.Arg16=
NR_158560.1:n.171G>A
NM_001355186.2:c.48G>A	NP_001342115.1:p.Arg16=
NM_016006.6:c.48G>A MANE Select	NP_057090.2:p.Arg16=