Canonical Allele Identifier: CA1360918349

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43720501A= , CM000665.2:g.43720501A=	GRCh38
NC_000003.11:g.43761993A= , CM000665.1:g.43761993A=	GRCh37
NC_000003.10:g.43736997A=	NCBI36
NG_007090.3:g.34619A=
NG_007090.5:g.34632A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000454293.2:c.*29+1940A=	ENSP00000412014.2:n.*29+1940A=
ENST00000463153.2:c.306+1940A=
ENST00000643477.1:c.*2480A=	ENSP00000496220.1:n.*2480A=
ENST00000644371.2:c.*1969A= MANE Select	ENSP00000495778.1:n.*1969A=
ENST00000649763.1:c.*29+1940A=	ENSP00000497701.1:n.*29+1940A=
ENST00000463153.1:n.309+1940A=
NM_016006.4:c.*1969A=	NP_057090.2:n.*1969A=
XM_011533779.1:c.*1969A=	XP_011532081.1:n.*1969A=
XM_011533780.1:c.*1995A=	XP_011532082.1:n.*1995A=
XR_940447.1:n.2964A=
NM_001355186.1:c.*29+1940A=	NP_001342115.1:n.*29+1940A=
NM_001365649.1:c.*1969A=	NP_001352578.1:n.*1969A=
NM_001365650.1:c.*1995A=	NP_001352579.1:n.*1995A=
NM_016006.5:c.*1969A=	NP_057090.2:n.*1969A=
NR_158560.1:n.3030A=
NM_001355186.2:c.*29+1940A=	NP_001342115.1:n.*29+1940A=
NM_016006.6:c.*1969A= MANE Select	NP_057090.2:n.*1969A=