Canonical Allele Identifier: CA1360917164

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717786C= , CM000665.2:g.43717786C=	GRCh38
NC_000003.11:g.43759278C= , CM000665.1:g.43759278C=	GRCh37
NC_000003.10:g.43734282C=	NCBI36
NG_007090.3:g.31904C=
NG_007090.5:g.31917C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.288C=
ENST00000454293.2:c.766C=	ENSP00000412014.2:p.Arg256=
ENST00000458276.7:c.774-657C=	ENSP00000390849.3:n.774-657C=
ENST00000463153.2:c.116C=
ENST00000642351.1:c.766C=	ENSP00000494478.1:p.Arg256=
ENST00000643140.1:c.*251C=	ENSP00000495588.1:n.*251C=
ENST00000643477.1:c.*350C=	ENSP00000496220.1:n.*350C=
ENST00000643500.1:c.*90C=	ENSP00000494735.1:n.*90C=
ENST00000643520.1:n.1055C=
ENST00000644371.2:c.889C= MANE Select	ENSP00000495778.1:p.Arg297=
ENST00000646378.1:c.*939C=	ENSP00000495826.1:n.*939C=
ENST00000646799.1:c.*248-657C=	ENSP00000494829.1:n.*248-657C=
ENST00000649763.1:c.889C=	ENSP00000497701.1:p.Arg297=
ENST00000413300.1:c.290C=	ENSP00000392159.1:p.Pro97=
ENST00000458276.6:c.889C=	ENSP00000390849.2:p.Arg297=
ENST00000463153.1:n.119C=
NM_016006.4:c.889C=	NP_057090.2:p.Arg297=
XM_011533779.1:c.766C=	XP_011532081.1:p.Arg256=
XM_011533780.1:c.774-657C=	XP_011532082.1:n.774-657C=
XR_940447.1:n.834C=
NM_001355186.1:c.889C=	NP_001342115.1:p.Arg297=
NM_001365649.1:c.766C=	NP_001352578.1:p.Arg256=
NM_001365650.1:c.774-657C=	NP_001352579.1:n.774-657C=
NM_016006.5:c.889C=	NP_057090.2:p.Arg297=
NR_158560.1:n.900C=
NM_001355186.2:c.889C=	NP_001342115.1:p.Arg297=
NM_016006.6:c.889C= MANE Select	NP_057090.2:p.Arg297=