Canonical Allele Identifier: CA1360918400

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43720632T= , CM000665.2:g.43720632T=	GRCh38
NC_000003.11:g.43762124T= , CM000665.1:g.43762124T=	GRCh37
NC_000003.10:g.43737128T=	NCBI36
NG_007090.3:g.34750T=
NG_007090.5:g.34763T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454293.2:c.*29+2071T=	ENSP00000412014.2:n.*29+2071T=
ENST00000463153.2:c.306+2071T=
ENST00000643477.1:c.*2611T=	ENSP00000496220.1:n.*2611T=
ENST00000644371.2:c.*2100T= MANE Select	ENSP00000495778.1:n.*2100T=
ENST00000649763.1:c.*29+2071T=	ENSP00000497701.1:n.*29+2071T=
ENST00000463153.1:n.309+2071T=
NM_016006.4:c.*2100T=	NP_057090.2:n.*2100T=
XM_011533779.1:c.*2100T=	XP_011532081.1:n.*2100T=
XM_011533780.1:c.*2126T=	XP_011532082.1:n.*2126T=
XR_940447.1:n.3095T=
NM_001355186.1:c.*29+2071T=	NP_001342115.1:n.*29+2071T=
NM_001365649.1:c.*2100T=	NP_001352578.1:n.*2100T=
NM_001365650.1:c.*2126T=	NP_001352579.1:n.*2126T=
NM_016006.5:c.*2100T=	NP_057090.2:n.*2100T=
NR_158560.1:n.3161T=
NM_001355186.2:c.*29+2071T=	NP_001342115.1:n.*29+2071T=
NM_016006.6:c.*2100T= MANE Select	NP_057090.2:n.*2100T=