Canonical Allele Identifier: CA1360909770

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43699317C= , CM000665.2:g.43699317C=	GRCh38
NC_000003.11:g.43740809C= , CM000665.1:g.43740809C=	GRCh37
NC_000003.10:g.43715813C=	NCBI36
NG_007090.3:g.13435C=
NG_007090.5:g.13448C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013894.3:c.89C=	ENSP00000013894.2:p.Thr30=
ENST00000454293.2:c.-35C=	ENSP00000412014.2:n.-35C=
ENST00000458276.7:c.89C=	ENSP00000390849.3:p.Thr30=
ENST00000642351.1:c.-35C=	ENSP00000494478.1:n.-35C=
ENST00000643140.1:c.89C=	ENSP00000495588.1:p.Thr30=
ENST00000643477.1:c.89C=	ENSP00000496220.1:p.Thr30=
ENST00000643500.1:c.89C=	ENSP00000494735.1:p.Thr30=
ENST00000643520.1:n.137C=
ENST00000644371.2:c.89C= MANE Select	ENSP00000495778.1:p.Thr30=
ENST00000646378.1:c.*139C=	ENSP00000495826.1:n.*139C=
ENST00000646799.1:c.89C=	ENSP00000494829.1:p.Thr30=
ENST00000649763.1:c.89C=	ENSP00000497701.1:p.Thr30=
ENST00000013894.2:c.89C=	ENSP00000013894.2:p.Thr30=
ENST00000454293.1:c.-35C=	ENSP00000412014.1:n.-35C=
ENST00000456453.5:c.-35C=	ENSP00000391582.1:n.-35C=
ENST00000458276.6:c.89C=	ENSP00000390849.2:p.Thr30=
ENST00000486764.1:n.190C=
NM_016006.4:c.89C=	NP_057090.2:p.Thr30=
XM_011533779.1:c.-35C=	XP_011532081.1:n.-35C=
XM_011533780.1:c.89C=	XP_011532082.1:p.Thr30=
XR_940447.1:n.146C=
NM_001355186.1:c.89C=	NP_001342115.1:p.Thr30=
NM_001365649.1:c.-35C=	NP_001352578.1:n.-35C=
NM_001365650.1:c.89C=	NP_001352579.1:p.Thr30=
NM_016006.5:c.89C=	NP_057090.2:p.Thr30=
NR_158560.1:n.212C=
NM_001355186.2:c.89C=	NP_001342115.1:p.Thr30=
NM_016006.6:c.89C= MANE Select	NP_057090.2:p.Thr30=