Canonical Allele Identifier: CA1360917199

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717862G= , CM000665.2:g.43717862G=	GRCh38
NC_000003.11:g.43759354G= , CM000665.1:g.43759354G=	GRCh37
NC_000003.10:g.43734358G=	NCBI36
NG_007090.3:g.31980G=
NG_007090.5:g.31993G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.359+5G=
ENST00000454293.2:c.837+5G=	ENSP00000412014.2:n.837+5G=
ENST00000458276.7:c.774-581G=	ENSP00000390849.3:n.774-581G=
ENST00000463153.2:c.187+5G=
ENST00000642351.1:c.837+5G=	ENSP00000494478.1:n.837+5G=
ENST00000643140.1:c.*322+5G=	ENSP00000495588.1:n.*322+5G=
ENST00000643477.1:c.*421+5G=	ENSP00000496220.1:n.*421+5G=
ENST00000643500.1:c.*161+5G=	ENSP00000494735.1:n.*161+5G=
ENST00000643520.1:n.1126+5G=
ENST00000644371.2:c.960+5G= MANE Select	ENSP00000495778.1:n.960+5G=
ENST00000646378.1:c.*1010+5G=	ENSP00000495826.1:n.*1010+5G=
ENST00000646799.1:c.*248-581G=	ENSP00000494829.1:n.*248-581G=
ENST00000649763.1:c.960+5G=	ENSP00000497701.1:n.960+5G=
ENST00000413300.1:c.361+5G=	ENSP00000392159.1:n.361+5G=
ENST00000458276.6:c.960+5G=	ENSP00000390849.2:n.960+5G=
ENST00000463153.1:n.190+5G=
NM_016006.4:c.960+5G=	NP_057090.2:n.960+5G=
XM_011533779.1:c.837+5G=	XP_011532081.1:n.837+5G=
XM_011533780.1:c.774-581G=	XP_011532082.1:n.774-581G=
XR_940447.1:n.905+5G=
NM_001355186.1:c.960+5G=	NP_001342115.1:n.960+5G=
NM_001365649.1:c.837+5G=	NP_001352578.1:n.837+5G=
NM_001365650.1:c.774-581G=	NP_001352579.1:n.774-581G=
NM_016006.5:c.960+5G=	NP_057090.2:n.960+5G=
NR_158560.1:n.971+5G=
NM_001355186.2:c.960+5G=	NP_001342115.1:n.960+5G=
NM_016006.6:c.960+5G= MANE Select	NP_057090.2:n.960+5G=