Canonical Allele Identifier: CA2815628436

Gene: ABHD12

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25308202_25308203insAC , CM000682.2:g.25308202_25308203insAC	GRCh38
NC_000020.10:g.25288838_25288839insAC , CM000682.1:g.25288838_25288839insAC	GRCh37
NC_000020.9:g.25236838_25236839insAC	NCBI36
NG_028119.1:g.87781_87782insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339157.10:c.788-157_788-156insTG MANE Select	ENSP00000341408.5:n.788-157_788-156insTG
ENST00000376542.8:c.788-157_788-156insTG	ENSP00000365725.3:n.788-157_788-156insTG
ENST00000465694.2:c.242-157_242-156insTG	ENSP00000459278.2:n.242-157_242-156insTG
ENST00000671784.1:c.242-157_242-156insTG	ENSP00000500451.1:n.242-157_242-156insTG
ENST00000671858.1:c.242-157_242-156insTG	ENSP00000500550.1:n.242-157_242-156insTG
ENST00000672001.1:n.299-157_299-156insTG
ENST00000672114.1:c.242-157_242-156insTG	ENSP00000499945.1:n.242-157_242-156insTG
ENST00000672258.1:c.242-157_242-156insTG	ENSP00000499868.1:n.242-157_242-156insTG
ENST00000672331.1:c.242-157_242-156insTG	ENSP00000500286.1:n.242-157_242-156insTG
ENST00000672358.1:c.242-157_242-156insTG	ENSP00000500062.1:n.242-157_242-156insTG
ENST00000672406.1:c.*127-157_*127-156insTG	ENSP00000500208.1:n.*127-157_*127-156insTG
ENST00000672566.1:c.317-157_317-156insTG	ENSP00000500106.1:n.317-157_317-156insTG
ENST00000672596.1:c.242-157_242-156insTG	ENSP00000500290.1:n.242-157_242-156insTG
ENST00000672871.1:c.242-157_242-156insTG	ENSP00000499949.1:n.242-157_242-156insTG
ENST00000673094.1:c.242-157_242-156insTG	ENSP00000500257.1:n.242-157_242-156insTG
ENST00000673121.1:c.344-157_344-156insTG	ENSP00000499839.1:n.344-157_344-156insTG
ENST00000673227.1:c.242-157_242-156insTG	ENSP00000500514.1:n.242-157_242-156insTG
ENST00000673524.1:c.350-157_350-156insTG
ENST00000339157.9:c.788-157_788-156insTG	ENSP00000341408.5:n.788-157_788-156insTG
ENST00000376542.7:c.788-157_788-156insTG	ENSP00000365725.3:n.788-157_788-156insTG
ENST00000481556.1:n.442-157_442-156insTG
ENST00000491682.5:c.317-157_317-156insTG	ENSP00000459495.1:n.317-157_317-156insTG
ENST00000576316.5:c.92-157_92-156insTG	ENSP00000459121.1:n.92-157_92-156insTG
NM_001042472.2:c.788-157_788-156insTG	NP_001035937.1:n.788-157_788-156insTG
NM_015600.4:c.788-157_788-156insTG	NP_056415.1:n.788-157_788-156insTG
XM_005260698.1:c.788-157_788-156insTG	XP_005260755.1:n.788-157_788-156insTG
XM_005260699.3:c.788-157_788-156insTG	XP_005260756.1:n.788-157_788-156insTG
XM_005260700.1:c.317-157_317-156insTG	XP_005260757.1:n.317-157_317-156insTG
XM_011529214.1:c.788-157_788-156insTG	XP_011527516.1:n.788-157_788-156insTG
XM_011529215.1:c.317-157_317-156insTG	XP_011527517.1:n.317-157_317-156insTG
XM_011529216.1:c.317-157_317-156insTG	XP_011527518.1:n.317-157_317-156insTG
XM_011529217.1:c.131-157_131-156insTG	XP_011527519.1:n.131-157_131-156insTG
XM_011529218.1:c.131-157_131-156insTG	XP_011527520.1:n.131-157_131-156insTG
XM_011529214.2:c.788-157_788-156insTG	XP_011527516.1:n.788-157_788-156insTG
XM_017027796.1:c.317-157_317-156insTG	XP_016883285.1:n.317-157_317-156insTG
XR_002958465.1:n.798-157_798-156insTG
XR_002958466.1:n.918-157_918-156insTG
XR_002958467.1:n.477-157_477-156insTG
NM_001042472.3:c.788-157_788-156insTG MANE Select	NP_001035937.1:n.788-157_788-156insTG
NM_015600.5:c.788-157_788-156insTG	NP_056415.1:n.788-157_788-156insTG