Canonical Allele Identifier: CA352347762

Gene: ABHD5

Linked Data

• MyVariant Identifiers: chr3:g.43759313C>T (hg19) ; chr3:g.43717821C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43717821C>T , CM000665.2:g.43717821C>T	GRCh38
NC_000003.11:g.43759313C>T , CM000665.1:g.43759313C>T	GRCh37
NC_000003.10:g.43734317C>T	NCBI36
NG_007090.3:g.31939C>T
NG_007090.5:g.31952C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413300.2:c.323C>T
ENST00000454293.2:c.801C>T	ENSP00000412014.2:p.Ile267=
ENST00000458276.7:c.774-622C>T	ENSP00000390849.3:n.774-622C>T
ENST00000463153.2:c.151C>T
ENST00000642351.1:c.801C>T	ENSP00000494478.1:p.Ile267=
ENST00000643140.1:c.*286C>T	ENSP00000495588.1:n.*286C>T
ENST00000643477.1:c.*385C>T	ENSP00000496220.1:n.*385C>T
ENST00000643500.1:c.*125C>T	ENSP00000494735.1:n.*125C>T
ENST00000643520.1:n.1090C>T
ENST00000644371.2:c.924C>T MANE Select	ENSP00000495778.1:p.Ile308=
ENST00000646378.1:c.*974C>T	ENSP00000495826.1:n.*974C>T
ENST00000646799.1:c.*248-622C>T	ENSP00000494829.1:n.*248-622C>T
ENST00000649763.1:c.924C>T	ENSP00000497701.1:p.Ile308=
ENST00000413300.1:c.325C>T	ENSP00000392159.1:p.Pro109Ser
ENST00000458276.6:c.924C>T	ENSP00000390849.2:p.Ile308=
ENST00000463153.1:n.154C>T
NM_016006.4:c.924C>T	NP_057090.2:p.Ile308=
XM_011533779.1:c.801C>T	XP_011532081.1:p.Ile267=
XM_011533780.1:c.774-622C>T	XP_011532082.1:n.774-622C>T
XR_940447.1:n.869C>T
NM_001355186.1:c.924C>T	NP_001342115.1:p.Ile308=
NM_001365649.1:c.801C>T	NP_001352578.1:p.Ile267=
NM_001365650.1:c.774-622C>T	NP_001352579.1:n.774-622C>T
NM_016006.5:c.924C>T	NP_057090.2:p.Ile308=
NR_158560.1:n.935C>T
NM_001355186.2:c.924C>T	NP_001342115.1:p.Ile308=
NM_016006.6:c.924C>T MANE Select	NP_057090.2:p.Ile308=