Canonical Allele Identifier: CA1360918339

Gene: ABHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.43720485T= , CM000665.2:g.43720485T=	GRCh38
NC_000003.11:g.43761977T= , CM000665.1:g.43761977T=	GRCh37
NC_000003.10:g.43736981T=	NCBI36
NG_007090.3:g.34603T=
NG_007090.5:g.34616T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000454293.2:c.*29+1924T=	ENSP00000412014.2:n.*29+1924T=
ENST00000463153.2:c.306+1924T=
ENST00000643477.1:c.*2464T=	ENSP00000496220.1:n.*2464T=
ENST00000644371.2:c.*1953T= MANE Select	ENSP00000495778.1:n.*1953T=
ENST00000649763.1:c.*29+1924T=	ENSP00000497701.1:n.*29+1924T=
ENST00000463153.1:n.309+1924T=
NM_016006.4:c.*1953T=	NP_057090.2:n.*1953T=
XM_011533779.1:c.*1953T=	XP_011532081.1:n.*1953T=
XM_011533780.1:c.*1979T=	XP_011532082.1:n.*1979T=
XR_940447.1:n.2948T=
NM_001355186.1:c.*29+1924T=	NP_001342115.1:n.*29+1924T=
NM_001365649.1:c.*1953T=	NP_001352578.1:n.*1953T=
NM_001365650.1:c.*1979T=	NP_001352579.1:n.*1979T=
NM_016006.5:c.*1953T=	NP_057090.2:n.*1953T=
NR_158560.1:n.3014T=
NM_001355186.2:c.*29+1924T=	NP_001342115.1:n.*29+1924T=
NM_016006.6:c.*1953T= MANE Select	NP_057090.2:n.*1953T=