Canonical Allele Identifier: CA352347824

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759336A>T (hg19) ; chr3:g.43717844A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717844A>T , CM000665.2:g.43717844A>T	GRCh38
NC_000003.11:g.43759336A>T , CM000665.1:g.43759336A>T	GRCh37
NC_000003.10:g.43734340A>T	NCBI36
NG_007090.3:g.31962A>T
NG_007090.5:g.31975A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.346A>T
ENST00000454293.2:c.824A>T	ENSP00000412014.2:p.Tyr275Phe
ENST00000458276.7:c.774-599A>T	ENSP00000390849.3:n.774-599A>T
ENST00000463153.2:c.174A>T
ENST00000642351.1:c.824A>T	ENSP00000494478.1:p.Tyr275Phe
ENST00000643140.1:c.*309A>T	ENSP00000495588.1:n.*309A>T
ENST00000643477.1:c.*408A>T	ENSP00000496220.1:n.*408A>T
ENST00000643500.1:c.*148A>T	ENSP00000494735.1:n.*148A>T
ENST00000643520.1:n.1113A>T
ENST00000644371.2:c.947A>T MANE Select	ENSP00000495778.1:p.Tyr316Phe
ENST00000646378.1:c.*997A>T	ENSP00000495826.1:n.*997A>T
ENST00000646799.1:c.*248-599A>T	ENSP00000494829.1:n.*248-599A>T
ENST00000649763.1:c.947A>T	ENSP00000497701.1:p.Tyr316Phe
ENST00000413300.1:c.348A>T	ENSP00000392159.1:p.Ile116=
ENST00000458276.6:c.947A>T	ENSP00000390849.2:p.Tyr316Phe
ENST00000463153.1:n.177A>T
NM_016006.4:c.947A>T	NP_057090.2:p.Tyr316Phe
XM_011533779.1:c.824A>T	XP_011532081.1:p.Tyr275Phe
XM_011533780.1:c.774-599A>T	XP_011532082.1:n.774-599A>T
XR_940447.1:n.892A>T
NM_001355186.1:c.947A>T	NP_001342115.1:p.Tyr316Phe
NM_001365649.1:c.824A>T	NP_001352578.1:p.Tyr275Phe
NM_001365650.1:c.774-599A>T	NP_001352579.1:n.774-599A>T
NM_016006.5:c.947A>T	NP_057090.2:p.Tyr316Phe
NR_158560.1:n.958A>T
NM_001355186.2:c.947A>T	NP_001342115.1:p.Tyr316Phe
NM_016006.6:c.947A>T MANE Select	NP_057090.2:p.Tyr316Phe