Canonical Allele Identifier: CA2665311523

Gene: ABHD5

Linked Data

• gnomAD v4: 3-43720394-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43720394C>A , CM000665.2:g.43720394C>A	GRCh38
NC_000003.11:g.43761886C>A , CM000665.1:g.43761886C>A	GRCh37
NC_000003.10:g.43736890C>A	NCBI36
NG_007090.3:g.34512C>A
NG_007090.5:g.34525C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454293.2:c.*29+1833C>A	ENSP00000412014.2:n.*29+1833C>A
ENST00000463153.2:c.306+1833C>A
ENST00000643477.1:c.*2373C>A	ENSP00000496220.1:n.*2373C>A
ENST00000644371.2:c.*1862C>A MANE Select	ENSP00000495778.1:n.*1862C>A
ENST00000649763.1:c.*29+1833C>A	ENSP00000497701.1:n.*29+1833C>A
ENST00000463153.1:n.309+1833C>A
NM_016006.4:c.*1862C>A	NP_057090.2:n.*1862C>A
XM_011533779.1:c.*1862C>A	XP_011532081.1:n.*1862C>A
XM_011533780.1:c.*1888C>A	XP_011532082.1:n.*1888C>A
XR_940447.1:n.2857C>A
NM_001355186.1:c.*29+1833C>A	NP_001342115.1:n.*29+1833C>A
NM_001365649.1:c.*1862C>A	NP_001352578.1:n.*1862C>A
NM_001365650.1:c.*1888C>A	NP_001352579.1:n.*1888C>A
NM_016006.5:c.*1862C>A	NP_057090.2:n.*1862C>A
NR_158560.1:n.2923C>A
NM_001355186.2:c.*29+1833C>A	NP_001342115.1:n.*29+1833C>A
NM_016006.6:c.*1862C>A MANE Select	NP_057090.2:n.*1862C>A