Canonical Allele Identifier: CA2665311570

Gene: ABHD5

Linked Data

• gnomAD v4: 3-43720785-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43720785C>A , CM000665.2:g.43720785C>A	GRCh38
NC_000003.11:g.43762277C>A , CM000665.1:g.43762277C>A	GRCh37
NC_000003.10:g.43737281C>A	NCBI36
NG_007090.3:g.34903C>A
NG_007090.5:g.34916C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454293.2:c.*29+2224C>A	ENSP00000412014.2:n.*29+2224C>A
ENST00000463153.2:c.306+2224C>A
ENST00000643477.1:c.*2764C>A	ENSP00000496220.1:n.*2764C>A
ENST00000644371.2:c.*2253C>A MANE Select	ENSP00000495778.1:n.*2253C>A
ENST00000649763.1:c.*29+2224C>A	ENSP00000497701.1:n.*29+2224C>A
ENST00000463153.1:n.309+2224C>A
NM_016006.4:c.*2253C>A	NP_057090.2:n.*2253C>A
XM_011533779.1:c.*2253C>A	XP_011532081.1:n.*2253C>A
XM_011533780.1:c.*2279C>A	XP_011532082.1:n.*2279C>A
XR_940447.1:n.3248C>A
NM_001355186.1:c.*29+2224C>A	NP_001342115.1:n.*29+2224C>A
NM_001365649.1:c.*2253C>A	NP_001352578.1:n.*2253C>A
NM_001365650.1:c.*2279C>A	NP_001352579.1:n.*2279C>A
NM_016006.5:c.*2253C>A	NP_057090.2:n.*2253C>A
NR_158560.1:n.3314C>A
NM_001355186.2:c.*29+2224C>A	NP_001342115.1:n.*29+2224C>A
NM_016006.6:c.*2253C>A MANE Select	NP_057090.2:n.*2253C>A