Canonical Allele Identifier: CA352347423

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759176T>G (hg19) ; chr3:g.43717684T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717684T>G , CM000665.2:g.43717684T>G	GRCh38
NC_000003.11:g.43759176T>G , CM000665.1:g.43759176T>G	GRCh37
NC_000003.10:g.43734180T>G	NCBI36
NG_007090.3:g.31802T>G
NG_007090.5:g.31815T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-82T>G
ENST00000454293.2:c.664T>G	ENSP00000412014.2:p.Phe222Val
ENST00000458276.7:c.774-759T>G	ENSP00000390849.3:n.774-759T>G
ENST00000463153.2:c.14T>G
ENST00000642351.1:c.664T>G	ENSP00000494478.1:p.Phe222Val
ENST00000643140.1:c.*149T>G	ENSP00000495588.1:n.*149T>G
ENST00000643477.1:c.*248T>G	ENSP00000496220.1:n.*248T>G
ENST00000643500.1:c.675T>G	ENSP00000494735.1:p.Leu225=
ENST00000643520.1:n.953T>G
ENST00000644371.2:c.787T>G MANE Select	ENSP00000495778.1:p.Phe263Val
ENST00000646378.1:c.*837T>G	ENSP00000495826.1:n.*837T>G
ENST00000646799.1:c.*248-759T>G	ENSP00000494829.1:n.*248-759T>G
ENST00000649763.1:c.787T>G	ENSP00000497701.1:p.Phe263Val
ENST00000413300.1:c.270-82T>G	ENSP00000392159.1:n.270-82T>G
ENST00000458276.6:c.787T>G	ENSP00000390849.2:p.Phe263Val
ENST00000463153.1:n.17T>G
NM_016006.4:c.787T>G	NP_057090.2:p.Phe263Val
XM_011533779.1:c.664T>G	XP_011532081.1:p.Phe222Val
XM_011533780.1:c.774-759T>G	XP_011532082.1:n.774-759T>G
XR_940447.1:n.732T>G
NM_001355186.1:c.787T>G	NP_001342115.1:p.Phe263Val
NM_001365649.1:c.664T>G	NP_001352578.1:p.Phe222Val
NM_001365650.1:c.774-759T>G	NP_001352579.1:n.774-759T>G
NM_016006.5:c.787T>G	NP_057090.2:p.Phe263Val
NR_158560.1:n.798T>G
NM_001355186.2:c.787T>G	NP_001342115.1:p.Phe263Val
NM_016006.6:c.787T>G MANE Select	NP_057090.2:p.Phe263Val