Canonical Allele Identifier: CA1360917150

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717741G= , CM000665.2:g.43717741G=	GRCh38
NC_000003.11:g.43759233G= , CM000665.1:g.43759233G=	GRCh37
NC_000003.10:g.43734237G=	NCBI36
NG_007090.3:g.31859G=
NG_007090.5:g.31872G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-25G=
ENST00000454293.2:c.721G=	ENSP00000412014.2:p.Gly241=
ENST00000458276.7:c.774-702G=	ENSP00000390849.3:n.774-702G=
ENST00000463153.2:c.71G=
ENST00000642351.1:c.721G=	ENSP00000494478.1:p.Gly241=
ENST00000643140.1:c.*206G=	ENSP00000495588.1:n.*206G=
ENST00000643477.1:c.*305G=	ENSP00000496220.1:n.*305G=
ENST00000643500.1:c.*45G=	ENSP00000494735.1:n.*45G=
ENST00000643520.1:n.1010G=
ENST00000644371.2:c.844G= MANE Select	ENSP00000495778.1:p.Gly282=
ENST00000646378.1:c.*894G=	ENSP00000495826.1:n.*894G=
ENST00000646799.1:c.*248-702G=	ENSP00000494829.1:n.*248-702G=
ENST00000649763.1:c.844G=	ENSP00000497701.1:p.Gly282=
ENST00000413300.1:c.270-25G=	ENSP00000392159.1:n.270-25G=
ENST00000458276.6:c.844G=	ENSP00000390849.2:p.Gly282=
ENST00000463153.1:n.74G=
NM_016006.4:c.844G=	NP_057090.2:p.Gly282=
XM_011533779.1:c.721G=	XP_011532081.1:p.Gly241=
XM_011533780.1:c.774-702G=	XP_011532082.1:n.774-702G=
XR_940447.1:n.789G=
NM_001355186.1:c.844G=	NP_001342115.1:p.Gly282=
NM_001365649.1:c.721G=	NP_001352578.1:p.Gly241=
NM_001365650.1:c.774-702G=	NP_001352579.1:n.774-702G=
NM_016006.5:c.844G=	NP_057090.2:p.Gly282=
NR_158560.1:n.855G=
NM_001355186.2:c.844G=	NP_001342115.1:p.Gly282=
NM_016006.6:c.844G= MANE Select	NP_057090.2:p.Gly282=