Canonical Allele Identifier: CA352347553

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759234G>T (hg19) ; chr3:g.43717742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717742G>T , CM000665.2:g.43717742G>T	GRCh38
NC_000003.11:g.43759234G>T , CM000665.1:g.43759234G>T	GRCh37
NC_000003.10:g.43734238G>T	NCBI36
NG_007090.3:g.31860G>T
NG_007090.5:g.31873G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-24G>T
ENST00000454293.2:c.722G>T	ENSP00000412014.2:p.Gly241Val
ENST00000458276.7:c.774-701G>T	ENSP00000390849.3:n.774-701G>T
ENST00000463153.2:c.72G>T
ENST00000642351.1:c.722G>T	ENSP00000494478.1:p.Gly241Val
ENST00000643140.1:c.*207G>T	ENSP00000495588.1:n.*207G>T
ENST00000643477.1:c.*306G>T	ENSP00000496220.1:n.*306G>T
ENST00000643500.1:c.*46G>T	ENSP00000494735.1:n.*46G>T
ENST00000643520.1:n.1011G>T
ENST00000644371.2:c.845G>T MANE Select	ENSP00000495778.1:p.Gly282Val
ENST00000646378.1:c.*895G>T	ENSP00000495826.1:n.*895G>T
ENST00000646799.1:c.*248-701G>T	ENSP00000494829.1:n.*248-701G>T
ENST00000649763.1:c.845G>T	ENSP00000497701.1:p.Gly282Val
ENST00000413300.1:c.270-24G>T	ENSP00000392159.1:n.270-24G>T
ENST00000458276.6:c.845G>T	ENSP00000390849.2:p.Gly282Val
ENST00000463153.1:n.75G>T
NM_016006.4:c.845G>T	NP_057090.2:p.Gly282Val
XM_011533779.1:c.722G>T	XP_011532081.1:p.Gly241Val
XM_011533780.1:c.774-701G>T	XP_011532082.1:n.774-701G>T
XR_940447.1:n.790G>T
NM_001355186.1:c.845G>T	NP_001342115.1:p.Gly282Val
NM_001365649.1:c.722G>T	NP_001352578.1:p.Gly241Val
NM_001365650.1:c.774-701G>T	NP_001352579.1:n.774-701G>T
NM_016006.5:c.845G>T	NP_057090.2:p.Gly282Val
NR_158560.1:n.856G>T
NM_001355186.2:c.845G>T	NP_001342115.1:p.Gly282Val
NM_016006.6:c.845G>T MANE Select	NP_057090.2:p.Gly282Val