Canonical Allele Identifier: CA1360918407

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43720648C= , CM000665.2:g.43720648C=	GRCh38
NC_000003.11:g.43762140C= , CM000665.1:g.43762140C=	GRCh37
NC_000003.10:g.43737144C=	NCBI36
NG_007090.3:g.34766C=
NG_007090.5:g.34779C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454293.2:c.*29+2087C=	ENSP00000412014.2:n.*29+2087C=
ENST00000463153.2:c.306+2087C=
ENST00000643477.1:c.*2627C=	ENSP00000496220.1:n.*2627C=
ENST00000644371.2:c.*2116C= MANE Select	ENSP00000495778.1:n.*2116C=
ENST00000649763.1:c.*29+2087C=	ENSP00000497701.1:n.*29+2087C=
ENST00000463153.1:n.309+2087C=
NM_016006.4:c.*2116C=	NP_057090.2:n.*2116C=
XM_011533779.1:c.*2116C=	XP_011532081.1:n.*2116C=
XM_011533780.1:c.*2142C=	XP_011532082.1:n.*2142C=
XR_940447.1:n.3111C=
NM_001355186.1:c.*29+2087C=	NP_001342115.1:n.*29+2087C=
NM_001365649.1:c.*2116C=	NP_001352578.1:n.*2116C=
NM_001365650.1:c.*2142C=	NP_001352579.1:n.*2142C=
NM_016006.5:c.*2116C=	NP_057090.2:n.*2116C=
NR_158560.1:n.3177C=
NM_001355186.2:c.*29+2087C=	NP_001342115.1:n.*29+2087C=
NM_016006.6:c.*2116C= MANE Select	NP_057090.2:n.*2116C=