Canonical Allele Identifier: CA1360917166

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717791C= , CM000665.2:g.43717791C=	GRCh38
NC_000003.11:g.43759283C= , CM000665.1:g.43759283C=	GRCh37
NC_000003.10:g.43734287C=	NCBI36
NG_007090.3:g.31909C=
NG_007090.5:g.31922C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.293C=
ENST00000454293.2:c.771C=	ENSP00000412014.2:p.Ser257=
ENST00000458276.7:c.774-652C=	ENSP00000390849.3:n.774-652C=
ENST00000463153.2:c.121C=
ENST00000642351.1:c.771C=	ENSP00000494478.1:p.Ser257=
ENST00000643140.1:c.*256C=	ENSP00000495588.1:n.*256C=
ENST00000643477.1:c.*355C=	ENSP00000496220.1:n.*355C=
ENST00000643500.1:c.*95C=	ENSP00000494735.1:n.*95C=
ENST00000643520.1:n.1060C=
ENST00000644371.2:c.894C= MANE Select	ENSP00000495778.1:p.Ser298=
ENST00000646378.1:c.*944C=	ENSP00000495826.1:n.*944C=
ENST00000646799.1:c.*248-652C=	ENSP00000494829.1:n.*248-652C=
ENST00000649763.1:c.894C=	ENSP00000497701.1:p.Ser298=
ENST00000413300.1:c.295C=	ENSP00000392159.1:p.Leu99=
ENST00000458276.6:c.894C=	ENSP00000390849.2:p.Ser298=
ENST00000463153.1:n.124C=
NM_016006.4:c.894C=	NP_057090.2:p.Ser298=
XM_011533779.1:c.771C=	XP_011532081.1:p.Ser257=
XM_011533780.1:c.774-652C=	XP_011532082.1:n.774-652C=
XR_940447.1:n.839C=
NM_001355186.1:c.894C=	NP_001342115.1:p.Ser298=
NM_001365649.1:c.771C=	NP_001352578.1:p.Ser257=
NM_001365650.1:c.774-652C=	NP_001352579.1:n.774-652C=
NM_016006.5:c.894C=	NP_057090.2:p.Ser298=
NR_158560.1:n.905C=
NM_001355186.2:c.894C=	NP_001342115.1:p.Ser298=
NM_016006.6:c.894C= MANE Select	NP_057090.2:p.Ser298=