Canonical Allele Identifier: CA433379439

Gene: ABHD5

Linked Data

• dbSNP Id: rs1258269238
• gnomAD v2: 3-43759383-T-C
• gnomAD v3: 3-43717891-T-C
• gnomAD v4: 3-43717891-T-C
• MyVariant Identifiers: chr3:g.43759383T>C (hg19) ; chr3:g.43717891T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717891T>C , CM000665.2:g.43717891T>C	GRCh38
NC_000003.11:g.43759383T>C , CM000665.1:g.43759383T>C	GRCh37
NC_000003.10:g.43734387T>C	NCBI36
NG_007090.3:g.32009T>C
NG_007090.5:g.32022T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.359+34T>C
ENST00000454293.2:c.837+34T>C	ENSP00000412014.2:n.837+34T>C
ENST00000458276.7:c.774-552T>C	ENSP00000390849.3:n.774-552T>C
ENST00000463153.2:c.187+34T>C
ENST00000642351.1:c.837+34T>C	ENSP00000494478.1:n.837+34T>C
ENST00000643140.1:c.*322+34T>C	ENSP00000495588.1:n.*322+34T>C
ENST00000643477.1:c.*421+34T>C	ENSP00000496220.1:n.*421+34T>C
ENST00000643500.1:c.*161+34T>C	ENSP00000494735.1:n.*161+34T>C
ENST00000643520.1:n.1126+34T>C
ENST00000644371.2:c.960+34T>C MANE Select	ENSP00000495778.1:n.960+34T>C
ENST00000646378.1:c.*1010+34T>C	ENSP00000495826.1:n.*1010+34T>C
ENST00000646799.1:c.*248-552T>C	ENSP00000494829.1:n.*248-552T>C
ENST00000649763.1:c.960+34T>C	ENSP00000497701.1:n.960+34T>C
ENST00000413300.1:c.361+34T>C	ENSP00000392159.1:n.361+34T>C
ENST00000458276.6:c.960+34T>C	ENSP00000390849.2:n.960+34T>C
ENST00000463153.1:n.190+34T>C
NM_016006.4:c.960+34T>C	NP_057090.2:n.960+34T>C
XM_011533779.1:c.837+34T>C	XP_011532081.1:n.837+34T>C
XM_011533780.1:c.774-552T>C	XP_011532082.1:n.774-552T>C
XR_940447.1:n.905+34T>C
NM_001355186.1:c.960+34T>C	NP_001342115.1:n.960+34T>C
NM_001365649.1:c.837+34T>C	NP_001352578.1:n.837+34T>C
NM_001365650.1:c.774-552T>C	NP_001352579.1:n.774-552T>C
NM_016006.5:c.960+34T>C	NP_057090.2:n.960+34T>C
NR_158560.1:n.971+34T>C
NM_001355186.2:c.960+34T>C	NP_001342115.1:n.960+34T>C
NM_016006.6:c.960+34T>C MANE Select	NP_057090.2:n.960+34T>C