Canonical Allele Identifier: CA433379406

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759208A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717716A>C , CM000665.2:g.43717716A>C	GRCh38
NC_000003.11:g.43759208A>C , CM000665.1:g.43759208A>C	GRCh37
NC_000003.10:g.43734212A>C	NCBI36
NG_007090.3:g.31834A>C
NG_007090.5:g.31847A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000413300.2:c.268-50A>C
ENST00000454293.2:c.696A>C	ENSP00000412014.2:p.Ala232=
ENST00000458276.7:c.774-727A>C	ENSP00000390849.3:n.774-727A>C
ENST00000463153.2:c.46A>C
ENST00000642351.1:c.696A>C	ENSP00000494478.1:p.Ala232=
ENST00000643140.1:c.*181A>C	ENSP00000495588.1:n.*181A>C
ENST00000643477.1:c.*280A>C	ENSP00000496220.1:n.*280A>C
ENST00000643500.1:c.*20A>C	ENSP00000494735.1:n.*20A>C
ENST00000643520.1:n.985A>C
ENST00000644371.2:c.819A>C MANE Select	ENSP00000495778.1:p.Ala273=
ENST00000646378.1:c.*869A>C	ENSP00000495826.1:n.*869A>C
ENST00000646799.1:c.*248-727A>C	ENSP00000494829.1:n.*248-727A>C
ENST00000649763.1:c.819A>C	ENSP00000497701.1:p.Ala273=
ENST00000413300.1:c.270-50A>C	ENSP00000392159.1:n.270-50A>C
ENST00000458276.6:c.819A>C	ENSP00000390849.2:p.Ala273=
ENST00000463153.1:n.49A>C
NM_016006.4:c.819A>C	NP_057090.2:p.Ala273=
XM_011533779.1:c.696A>C	XP_011532081.1:p.Ala232=
XM_011533780.1:c.774-727A>C	XP_011532082.1:n.774-727A>C
XR_940447.1:n.764A>C
NM_001355186.1:c.819A>C	NP_001342115.1:p.Ala273=
NM_001365649.1:c.696A>C	NP_001352578.1:p.Ala232=
NM_001365650.1:c.774-727A>C	NP_001352579.1:n.774-727A>C
NM_016006.5:c.819A>C	NP_057090.2:p.Ala273=
NR_158560.1:n.830A>C
NM_001355186.2:c.819A>C	NP_001342115.1:p.Ala273=
NM_016006.6:c.819A>C MANE Select	NP_057090.2:p.Ala273=