Canonical Allele Identifier: CA907390492

Gene: ABHD5

Linked Data

• dbSNP Id: rs1415022999
• gnomAD v3: 3-43717886-A-G
• gnomAD v4: 3-43717886-A-G
• MyVariant Identifiers: chr3:g.43759378A>G (hg19) ; chr3:g.43717886A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717886A>G , CM000665.2:g.43717886A>G	GRCh38
NC_000003.11:g.43759378A>G , CM000665.1:g.43759378A>G	GRCh37
NC_000003.10:g.43734382A>G	NCBI36
NG_007090.3:g.32004A>G
NG_007090.5:g.32017A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.359+29A>G
ENST00000454293.2:c.837+29A>G	ENSP00000412014.2:n.837+29A>G
ENST00000458276.7:c.774-557A>G	ENSP00000390849.3:n.774-557A>G
ENST00000463153.2:c.187+29A>G
ENST00000642351.1:c.837+29A>G	ENSP00000494478.1:n.837+29A>G
ENST00000643140.1:c.*322+29A>G	ENSP00000495588.1:n.*322+29A>G
ENST00000643477.1:c.*421+29A>G	ENSP00000496220.1:n.*421+29A>G
ENST00000643500.1:c.*161+29A>G	ENSP00000494735.1:n.*161+29A>G
ENST00000643520.1:n.1126+29A>G
ENST00000644371.2:c.960+29A>G MANE Select	ENSP00000495778.1:n.960+29A>G
ENST00000646378.1:c.*1010+29A>G	ENSP00000495826.1:n.*1010+29A>G
ENST00000646799.1:c.*248-557A>G	ENSP00000494829.1:n.*248-557A>G
ENST00000649763.1:c.960+29A>G	ENSP00000497701.1:n.960+29A>G
ENST00000413300.1:c.361+29A>G	ENSP00000392159.1:n.361+29A>G
ENST00000458276.6:c.960+29A>G	ENSP00000390849.2:n.960+29A>G
ENST00000463153.1:n.190+29A>G
NM_016006.4:c.960+29A>G	NP_057090.2:n.960+29A>G
XM_011533779.1:c.837+29A>G	XP_011532081.1:n.837+29A>G
XM_011533780.1:c.774-557A>G	XP_011532082.1:n.774-557A>G
XR_940447.1:n.905+29A>G
NM_001355186.1:c.960+29A>G	NP_001342115.1:n.960+29A>G
NM_001365649.1:c.837+29A>G	NP_001352578.1:n.837+29A>G
NM_001365650.1:c.774-557A>G	NP_001352579.1:n.774-557A>G
NM_016006.5:c.960+29A>G	NP_057090.2:n.960+29A>G
NR_158560.1:n.971+29A>G
NM_001355186.2:c.960+29A>G	NP_001342115.1:n.960+29A>G
NM_016006.6:c.960+29A>G MANE Select	NP_057090.2:n.960+29A>G