Canonical Allele Identifier: CA352347523

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759219T>G (hg19) ; chr3:g.43717727T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717727T>G , CM000665.2:g.43717727T>G	GRCh38
NC_000003.11:g.43759219T>G , CM000665.1:g.43759219T>G	GRCh37
NC_000003.10:g.43734223T>G	NCBI36
NG_007090.3:g.31845T>G
NG_007090.5:g.31858T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.268-39T>G
ENST00000454293.2:c.707T>G	ENSP00000412014.2:p.Met236Arg
ENST00000458276.7:c.774-716T>G	ENSP00000390849.3:n.774-716T>G
ENST00000463153.2:c.57T>G
ENST00000642351.1:c.707T>G	ENSP00000494478.1:p.Met236Arg
ENST00000643140.1:c.*192T>G	ENSP00000495588.1:n.*192T>G
ENST00000643477.1:c.*291T>G	ENSP00000496220.1:n.*291T>G
ENST00000643500.1:c.*31T>G	ENSP00000494735.1:n.*31T>G
ENST00000643520.1:n.996T>G
ENST00000644371.2:c.830T>G MANE Select	ENSP00000495778.1:p.Met277Arg
ENST00000646378.1:c.*880T>G	ENSP00000495826.1:n.*880T>G
ENST00000646799.1:c.*248-716T>G	ENSP00000494829.1:n.*248-716T>G
ENST00000649763.1:c.830T>G	ENSP00000497701.1:p.Met277Arg
ENST00000413300.1:c.270-39T>G	ENSP00000392159.1:n.270-39T>G
ENST00000458276.6:c.830T>G	ENSP00000390849.2:p.Met277Arg
ENST00000463153.1:n.60T>G
NM_016006.4:c.830T>G	NP_057090.2:p.Met277Arg
XM_011533779.1:c.707T>G	XP_011532081.1:p.Met236Arg
XM_011533780.1:c.774-716T>G	XP_011532082.1:n.774-716T>G
XR_940447.1:n.775T>G
NM_001355186.1:c.830T>G	NP_001342115.1:p.Met277Arg
NM_001365649.1:c.707T>G	NP_001352578.1:p.Met236Arg
NM_001365650.1:c.774-716T>G	NP_001352579.1:n.774-716T>G
NM_016006.5:c.830T>G	NP_057090.2:p.Met277Arg
NR_158560.1:n.841T>G
NM_001355186.2:c.830T>G	NP_001342115.1:p.Met277Arg
NM_016006.6:c.830T>G MANE Select	NP_057090.2:p.Met277Arg