Canonical Allele Identifier: CA352347532

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759222T>C (hg19) ; chr3:g.43717730T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717730T>C , CM000665.2:g.43717730T>C	GRCh38
NC_000003.11:g.43759222T>C , CM000665.1:g.43759222T>C	GRCh37
NC_000003.10:g.43734226T>C	NCBI36
NG_007090.3:g.31848T>C
NG_007090.5:g.31861T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-36T>C
ENST00000454293.2:c.710T>C	ENSP00000412014.2:p.Leu237Pro
ENST00000458276.7:c.774-713T>C	ENSP00000390849.3:n.774-713T>C
ENST00000463153.2:c.60T>C
ENST00000642351.1:c.710T>C	ENSP00000494478.1:p.Leu237Pro
ENST00000643140.1:c.*195T>C	ENSP00000495588.1:n.*195T>C
ENST00000643477.1:c.*294T>C	ENSP00000496220.1:n.*294T>C
ENST00000643500.1:c.*34T>C	ENSP00000494735.1:n.*34T>C
ENST00000643520.1:n.999T>C
ENST00000644371.2:c.833T>C MANE Select	ENSP00000495778.1:p.Leu278Pro
ENST00000646378.1:c.*883T>C	ENSP00000495826.1:n.*883T>C
ENST00000646799.1:c.*248-713T>C	ENSP00000494829.1:n.*248-713T>C
ENST00000649763.1:c.833T>C	ENSP00000497701.1:p.Leu278Pro
ENST00000413300.1:c.270-36T>C	ENSP00000392159.1:n.270-36T>C
ENST00000458276.6:c.833T>C	ENSP00000390849.2:p.Leu278Pro
ENST00000463153.1:n.63T>C
NM_016006.4:c.833T>C	NP_057090.2:p.Leu278Pro
XM_011533779.1:c.710T>C	XP_011532081.1:p.Leu237Pro
XM_011533780.1:c.774-713T>C	XP_011532082.1:n.774-713T>C
XR_940447.1:n.778T>C
NM_001355186.1:c.833T>C	NP_001342115.1:p.Leu278Pro
NM_001365649.1:c.710T>C	NP_001352578.1:p.Leu237Pro
NM_001365650.1:c.774-713T>C	NP_001352579.1:n.774-713T>C
NM_016006.5:c.833T>C	NP_057090.2:p.Leu278Pro
NR_158560.1:n.844T>C
NM_001355186.2:c.833T>C	NP_001342115.1:p.Leu278Pro
NM_016006.6:c.833T>C MANE Select	NP_057090.2:p.Leu278Pro