Canonical Allele Identifier: CA1360917152

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717749G= , CM000665.2:g.43717749G=	GRCh38
NC_000003.11:g.43759241G= , CM000665.1:g.43759241G=	GRCh37
NC_000003.10:g.43734245G=	NCBI36
NG_007090.3:g.31867G=
NG_007090.5:g.31880G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-17G=
ENST00000454293.2:c.729G=	ENSP00000412014.2:p.Met243=
ENST00000458276.7:c.774-694G=	ENSP00000390849.3:n.774-694G=
ENST00000463153.2:c.79G=
ENST00000642351.1:c.729G=	ENSP00000494478.1:p.Met243=
ENST00000643140.1:c.*214G=	ENSP00000495588.1:n.*214G=
ENST00000643477.1:c.*313G=	ENSP00000496220.1:n.*313G=
ENST00000643500.1:c.*53G=	ENSP00000494735.1:n.*53G=
ENST00000643520.1:n.1018G=
ENST00000644371.2:c.852G= MANE Select	ENSP00000495778.1:p.Met284=
ENST00000646378.1:c.*902G=	ENSP00000495826.1:n.*902G=
ENST00000646799.1:c.*248-694G=	ENSP00000494829.1:n.*248-694G=
ENST00000649763.1:c.852G=	ENSP00000497701.1:p.Met284=
ENST00000413300.1:c.270-17G=	ENSP00000392159.1:n.270-17G=
ENST00000458276.6:c.852G=	ENSP00000390849.2:p.Met284=
ENST00000463153.1:n.82G=
NM_016006.4:c.852G=	NP_057090.2:p.Met284=
XM_011533779.1:c.729G=	XP_011532081.1:p.Met243=
XM_011533780.1:c.774-694G=	XP_011532082.1:n.774-694G=
XR_940447.1:n.797G=
NM_001355186.1:c.852G=	NP_001342115.1:p.Met284=
NM_001365649.1:c.729G=	NP_001352578.1:p.Met243=
NM_001365650.1:c.774-694G=	NP_001352579.1:n.774-694G=
NM_016006.5:c.852G=	NP_057090.2:p.Met284=
NR_158560.1:n.863G=
NM_001355186.2:c.852G=	NP_001342115.1:p.Met284=
NM_016006.6:c.852G= MANE Select	NP_057090.2:p.Met284=