Canonical Allele Identifier: CA352347514

Gene: ABHD5

Linked Data

• dbSNP Id: rs1180140883
• gnomAD v2: 3-43759215-C-T
• gnomAD v4: 3-43717723-C-T
• MyVariant Identifiers: chr3:g.43759215C>T (hg19) ; chr3:g.43717723C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717723C>T , CM000665.2:g.43717723C>T	GRCh38
NC_000003.11:g.43759215C>T , CM000665.1:g.43759215C>T	GRCh37
NC_000003.10:g.43734219C>T	NCBI36
NG_007090.3:g.31841C>T
NG_007090.5:g.31854C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-43C>T
ENST00000454293.2:c.703C>T	ENSP00000412014.2:p.Pro235Ser
ENST00000458276.7:c.774-720C>T	ENSP00000390849.3:n.774-720C>T
ENST00000463153.2:c.53C>T
ENST00000642351.1:c.703C>T	ENSP00000494478.1:p.Pro235Ser
ENST00000643140.1:c.*188C>T	ENSP00000495588.1:n.*188C>T
ENST00000643477.1:c.*287C>T	ENSP00000496220.1:n.*287C>T
ENST00000643500.1:c.*27C>T	ENSP00000494735.1:n.*27C>T
ENST00000643520.1:n.992C>T
ENST00000644371.2:c.826C>T MANE Select	ENSP00000495778.1:p.Pro276Ser
ENST00000646378.1:c.*876C>T	ENSP00000495826.1:n.*876C>T
ENST00000646799.1:c.*248-720C>T	ENSP00000494829.1:n.*248-720C>T
ENST00000649763.1:c.826C>T	ENSP00000497701.1:p.Pro276Ser
ENST00000413300.1:c.270-43C>T	ENSP00000392159.1:n.270-43C>T
ENST00000458276.6:c.826C>T	ENSP00000390849.2:p.Pro276Ser
ENST00000463153.1:n.56C>T
NM_016006.4:c.826C>T	NP_057090.2:p.Pro276Ser
XM_011533779.1:c.703C>T	XP_011532081.1:p.Pro235Ser
XM_011533780.1:c.774-720C>T	XP_011532082.1:n.774-720C>T
XR_940447.1:n.771C>T
NM_001355186.1:c.826C>T	NP_001342115.1:p.Pro276Ser
NM_001365649.1:c.703C>T	NP_001352578.1:p.Pro235Ser
NM_001365650.1:c.774-720C>T	NP_001352579.1:n.774-720C>T
NM_016006.5:c.826C>T	NP_057090.2:p.Pro276Ser
NR_158560.1:n.837C>T
NM_001355186.2:c.826C>T	NP_001342115.1:p.Pro276Ser
NM_016006.6:c.826C>T MANE Select	NP_057090.2:p.Pro276Ser