Canonical Allele Identifier: CA1360917122

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717675G= , CM000665.2:g.43717675G=	GRCh38
NC_000003.11:g.43759167G= , CM000665.1:g.43759167G=	GRCh37
NC_000003.10:g.43734171G=	NCBI36
NG_007090.3:g.31793G=
NG_007090.5:g.31806G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-91G=
ENST00000454293.2:c.655G=	ENSP00000412014.2:p.Glu219=
ENST00000458276.7:c.774-768G=	ENSP00000390849.3:n.774-768G=
ENST00000463153.2:c.5G=
ENST00000642351.1:c.655G=	ENSP00000494478.1:p.Glu219=
ENST00000643140.1:c.*140G=	ENSP00000495588.1:n.*140G=
ENST00000643477.1:c.*239G=	ENSP00000496220.1:n.*239G=
ENST00000643500.1:c.666G=	ENSP00000494735.1:p.Val222=
ENST00000643520.1:n.944G=
ENST00000644371.2:c.778G= MANE Select	ENSP00000495778.1:p.Glu260=
ENST00000646378.1:c.*828G=	ENSP00000495826.1:n.*828G=
ENST00000646799.1:c.*248-768G=	ENSP00000494829.1:n.*248-768G=
ENST00000649763.1:c.778G=	ENSP00000497701.1:p.Glu260=
ENST00000413300.1:c.270-91G=	ENSP00000392159.1:n.270-91G=
ENST00000458276.6:c.778G=	ENSP00000390849.2:p.Glu260=
ENST00000463153.1:n.8G=
NM_016006.4:c.778G=	NP_057090.2:p.Glu260=
XM_011533779.1:c.655G=	XP_011532081.1:p.Glu219=
XM_011533780.1:c.774-768G=	XP_011532082.1:n.774-768G=
XR_940447.1:n.723G=
NM_001355186.1:c.778G=	NP_001342115.1:p.Glu260=
NM_001365649.1:c.655G=	NP_001352578.1:p.Glu219=
NM_001365650.1:c.774-768G=	NP_001352579.1:n.774-768G=
NM_016006.5:c.778G=	NP_057090.2:p.Glu260=
NR_158560.1:n.789G=
NM_001355186.2:c.778G=	NP_001342115.1:p.Glu260=
NM_016006.6:c.778G= MANE Select	NP_057090.2:p.Glu260=