Canonical Allele Identifier: CA352347426

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759177T>G (hg19) ; chr3:g.43717685T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717685T>G , CM000665.2:g.43717685T>G	GRCh38
NC_000003.11:g.43759177T>G , CM000665.1:g.43759177T>G	GRCh37
NC_000003.10:g.43734181T>G	NCBI36
NG_007090.3:g.31803T>G
NG_007090.5:g.31816T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-81T>G
ENST00000454293.2:c.665T>G	ENSP00000412014.2:p.Phe222Cys
ENST00000458276.7:c.774-758T>G	ENSP00000390849.3:n.774-758T>G
ENST00000463153.2:c.15T>G
ENST00000642351.1:c.665T>G	ENSP00000494478.1:p.Phe222Cys
ENST00000643140.1:c.*150T>G	ENSP00000495588.1:n.*150T>G
ENST00000643477.1:c.*249T>G	ENSP00000496220.1:n.*249T>G
ENST00000643500.1:c.676T>G	ENSP00000494735.1:p.Ser226Ala
ENST00000643520.1:n.954T>G
ENST00000644371.2:c.788T>G MANE Select	ENSP00000495778.1:p.Phe263Cys
ENST00000646378.1:c.*838T>G	ENSP00000495826.1:n.*838T>G
ENST00000646799.1:c.*248-758T>G	ENSP00000494829.1:n.*248-758T>G
ENST00000649763.1:c.788T>G	ENSP00000497701.1:p.Phe263Cys
ENST00000413300.1:c.270-81T>G	ENSP00000392159.1:n.270-81T>G
ENST00000458276.6:c.788T>G	ENSP00000390849.2:p.Phe263Cys
ENST00000463153.1:n.18T>G
NM_016006.4:c.788T>G	NP_057090.2:p.Phe263Cys
XM_011533779.1:c.665T>G	XP_011532081.1:p.Phe222Cys
XM_011533780.1:c.774-758T>G	XP_011532082.1:n.774-758T>G
XR_940447.1:n.733T>G
NM_001355186.1:c.788T>G	NP_001342115.1:p.Phe263Cys
NM_001365649.1:c.665T>G	NP_001352578.1:p.Phe222Cys
NM_001365650.1:c.774-758T>G	NP_001352579.1:n.774-758T>G
NM_016006.5:c.788T>G	NP_057090.2:p.Phe263Cys
NR_158560.1:n.799T>G
NM_001355186.2:c.788T>G	NP_001342115.1:p.Phe263Cys
NM_016006.6:c.788T>G MANE Select	NP_057090.2:p.Phe263Cys