Canonical Allele Identifier: CA352344743

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43740801G>T (hg19) ; chr3:g.43699309G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43699309G>T , CM000665.2:g.43699309G>T	GRCh38
NC_000003.11:g.43740801G>T , CM000665.1:g.43740801G>T	GRCh37
NC_000003.10:g.43715805G>T	NCBI36
NG_007090.3:g.13427G>T
NG_007090.5:g.13440G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013894.3:c.81G>T	ENSP00000013894.2:p.Trp27Cys
ENST00000454293.2:c.-43G>T	ENSP00000412014.2:n.-43G>T
ENST00000458276.7:c.81G>T	ENSP00000390849.3:p.Trp27Cys
ENST00000642351.1:c.-43G>T	ENSP00000494478.1:n.-43G>T
ENST00000643140.1:c.81G>T	ENSP00000495588.1:p.Trp27Cys
ENST00000643477.1:c.81G>T	ENSP00000496220.1:p.Trp27Cys
ENST00000643500.1:c.81G>T	ENSP00000494735.1:p.Trp27Cys
ENST00000643520.1:n.129G>T
ENST00000644371.2:c.81G>T MANE Select	ENSP00000495778.1:p.Trp27Cys
ENST00000646378.1:c.*131G>T	ENSP00000495826.1:n.*131G>T
ENST00000646799.1:c.81G>T	ENSP00000494829.1:p.Trp27Cys
ENST00000649763.1:c.81G>T	ENSP00000497701.1:p.Trp27Cys
ENST00000013894.2:c.81G>T	ENSP00000013894.2:p.Trp27Cys
ENST00000454293.1:c.-43G>T	ENSP00000412014.1:n.-43G>T
ENST00000456453.5:c.-43G>T	ENSP00000391582.1:n.-43G>T
ENST00000458276.6:c.81G>T	ENSP00000390849.2:p.Trp27Cys
ENST00000486764.1:n.182G>T
NM_016006.4:c.81G>T	NP_057090.2:p.Trp27Cys
XM_011533779.1:c.-43G>T	XP_011532081.1:n.-43G>T
XM_011533780.1:c.81G>T	XP_011532082.1:p.Trp27Cys
XR_940447.1:n.138G>T
NM_001355186.1:c.81G>T	NP_001342115.1:p.Trp27Cys
NM_001365649.1:c.-43G>T	NP_001352578.1:n.-43G>T
NM_001365650.1:c.81G>T	NP_001352579.1:p.Trp27Cys
NM_016006.5:c.81G>T	NP_057090.2:p.Trp27Cys
NR_158560.1:n.204G>T
NM_001355186.2:c.81G>T	NP_001342115.1:p.Trp27Cys
NM_016006.6:c.81G>T MANE Select	NP_057090.2:p.Trp27Cys