Canonical Allele Identifier: CA352347849

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759344A>T (hg19) ; chr3:g.43717852A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717852A>T , CM000665.2:g.43717852A>T	GRCh38
NC_000003.11:g.43759344A>T , CM000665.1:g.43759344A>T	GRCh37
NC_000003.10:g.43734348A>T	NCBI36
NG_007090.3:g.31970A>T
NG_007090.5:g.31983A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.354A>T
ENST00000454293.2:c.832A>T	ENSP00000412014.2:p.Thr278Ser
ENST00000458276.7:c.774-591A>T	ENSP00000390849.3:n.774-591A>T
ENST00000463153.2:c.182A>T
ENST00000642351.1:c.832A>T	ENSP00000494478.1:p.Thr278Ser
ENST00000643140.1:c.*317A>T	ENSP00000495588.1:n.*317A>T
ENST00000643477.1:c.*416A>T	ENSP00000496220.1:n.*416A>T
ENST00000643500.1:c.*156A>T	ENSP00000494735.1:n.*156A>T
ENST00000643520.1:n.1121A>T
ENST00000644371.2:c.955A>T MANE Select	ENSP00000495778.1:p.Thr319Ser
ENST00000646378.1:c.*1005A>T	ENSP00000495826.1:n.*1005A>T
ENST00000646799.1:c.*248-591A>T	ENSP00000494829.1:n.*248-591A>T
ENST00000649763.1:c.955A>T	ENSP00000497701.1:p.Thr319Ser
ENST00000413300.1:c.356A>T	ENSP00000392159.1:p.Asp119Val
ENST00000458276.6:c.955A>T	ENSP00000390849.2:p.Thr319Ser
ENST00000463153.1:n.185A>T
NM_016006.4:c.955A>T	NP_057090.2:p.Thr319Ser
XM_011533779.1:c.832A>T	XP_011532081.1:p.Thr278Ser
XM_011533780.1:c.774-591A>T	XP_011532082.1:n.774-591A>T
XR_940447.1:n.900A>T
NM_001355186.1:c.955A>T	NP_001342115.1:p.Thr319Ser
NM_001365649.1:c.832A>T	NP_001352578.1:p.Thr278Ser
NM_001365650.1:c.774-591A>T	NP_001352579.1:n.774-591A>T
NM_016006.5:c.955A>T	NP_057090.2:p.Thr319Ser
NR_158560.1:n.966A>T
NM_001355186.2:c.955A>T	NP_001342115.1:p.Thr319Ser
NM_016006.6:c.955A>T MANE Select	NP_057090.2:p.Thr319Ser