Canonical Allele Identifier: CA2573136975

Gene: ABHD5

Linked Data

• ClinVar Variation Id: 1394037
• ClinVar RCV Id: RCV001884689
• dbSNP Id: rs764691568

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43699367G>A , CM000665.2:g.43699367G>A	GRCh38
NC_000003.11:g.43740859G>A , CM000665.1:g.43740859G>A	GRCh37
NC_000003.10:g.43715863G>A	NCBI36
NG_007090.3:g.13485G>A
NG_007090.5:g.13498G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013894.3:c.133+6G>A	ENSP00000013894.2:n.133+6G>A
ENST00000454293.2:c.10+6G>A	ENSP00000412014.2:n.10+6G>A
ENST00000458276.7:c.133+6G>A	ENSP00000390849.3:n.133+6G>A
ENST00000642351.1:c.10+6G>A	ENSP00000494478.1:n.10+6G>A
ENST00000643140.1:c.133+6G>A	ENSP00000495588.1:n.133+6G>A
ENST00000643477.1:c.133+6G>A	ENSP00000496220.1:n.133+6G>A
ENST00000643500.1:c.133+6G>A	ENSP00000494735.1:n.133+6G>A
ENST00000643520.1:n.181+6G>A
ENST00000644371.2:c.133+6G>A MANE Select	ENSP00000495778.1:n.133+6G>A
ENST00000646378.1:c.*183+6G>A	ENSP00000495826.1:n.*183+6G>A
ENST00000646799.1:c.133+6G>A	ENSP00000494829.1:n.133+6G>A
ENST00000649763.1:c.133+6G>A	ENSP00000497701.1:n.133+6G>A
ENST00000013894.2:c.133+6G>A	ENSP00000013894.2:n.133+6G>A
ENST00000454293.1:c.10+6G>A	ENSP00000412014.1:n.10+6G>A
ENST00000456453.5:c.10+6G>A	ENSP00000391582.1:n.10+6G>A
ENST00000458276.6:c.133+6G>A	ENSP00000390849.2:n.133+6G>A
ENST00000486764.1:n.240G>A
NM_016006.4:c.133+6G>A	NP_057090.2:n.133+6G>A
XM_011533779.1:c.10+6G>A	XP_011532081.1:n.10+6G>A
XM_011533780.1:c.133+6G>A	XP_011532082.1:n.133+6G>A
XR_940447.1:n.190+6G>A
NM_001355186.1:c.133+6G>A	NP_001342115.1:n.133+6G>A
NM_001365649.1:c.10+6G>A	NP_001352578.1:n.10+6G>A
NM_001365650.1:c.133+6G>A	NP_001352579.1:n.133+6G>A
NM_016006.5:c.133+6G>A	NP_057090.2:n.133+6G>A
NR_158560.1:n.256+6G>A
NM_001355186.2:c.133+6G>A	NP_001342115.1:n.133+6G>A
NM_016006.6:c.133+6G>A MANE Select	NP_057090.2:n.133+6G>A