Canonical Allele Identifier: CA742456625

Gene: ABHD12

Linked Data

• dbSNP Id: rs1242433623
• MyVariant Identifiers: chr20:g.25288659_25288661del (hg19) ; chr20:g.25308023_25308025del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25308023_25308025del , CM000682.2:g.25308023_25308025del	GRCh38
NC_000020.10:g.25288659_25288661del , CM000682.1:g.25288659_25288661del	GRCh37
NC_000020.9:g.25236659_25236661del	NCBI36
NG_028119.1:g.87958_87960del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339157.10:c.808_810del MANE Select	ENSP00000341408.5:p.Ile270del
ENST00000376542.8:c.808_810del	ENSP00000365725.3:p.Ile270del
ENST00000465694.2:c.262_264del	ENSP00000459278.2:p.Ile88del
ENST00000671784.1:c.262_264del	ENSP00000500451.1:p.Ile88del
ENST00000671858.1:c.262_264del	ENSP00000500550.1:p.Ile88del
ENST00000672001.1:n.319_321del
ENST00000672114.1:c.262_264del	ENSP00000499945.1:p.Ile88del
ENST00000672258.1:c.262_264del	ENSP00000499868.1:p.Ile88del
ENST00000672331.1:c.262_264del	ENSP00000500286.1:p.Ile88del
ENST00000672358.1:c.262_264del	ENSP00000500062.1:p.Ile88del
ENST00000672406.1:c.*147_*149del	ENSP00000500208.1:n.*147_*149del
ENST00000672566.1:c.337_339del	ENSP00000500106.1:p.Ile113del
ENST00000672596.1:c.262_264del	ENSP00000500290.1:p.Ile88del
ENST00000672871.1:c.262_264del	ENSP00000499949.1:p.Ile88del
ENST00000673094.1:c.262_264del	ENSP00000500257.1:p.Ile88del
ENST00000673121.1:c.364_366del	ENSP00000499839.1:p.Ile122del
ENST00000673227.1:c.262_264del	ENSP00000500514.1:p.Ile88del
ENST00000673524.1:c.370_372del
ENST00000339157.9:c.808_810del	ENSP00000341408.5:p.Ile270del
ENST00000376542.7:c.808_810del	ENSP00000365725.3:p.Ile270del
ENST00000481556.1:n.462_464del
ENST00000491682.5:c.337_339del	ENSP00000459495.1:p.Ile113del
ENST00000576316.5:c.112_114del	ENSP00000459121.1:p.Ile38del
NM_001042472.2:c.808_810del	NP_001035937.1:p.Ile270del
NM_015600.4:c.808_810del	NP_056415.1:p.Ile270del
XM_005260698.1:c.808_810del	XP_005260755.1:p.Ile270del
XM_005260699.3:c.808_810del	XP_005260756.1:p.Ile270del
XM_005260700.1:c.337_339del	XP_005260757.1:p.Ile113del
XM_011529214.1:c.808_810del	XP_011527516.1:p.Ile270del
XM_011529215.1:c.337_339del	XP_011527517.1:p.Ile113del
XM_011529216.1:c.337_339del	XP_011527518.1:p.Ile113del
XM_011529217.1:c.151_153del	XP_011527519.1:p.Ile51del
XM_011529218.1:c.151_153del	XP_011527520.1:p.Ile51del
XM_011529214.2:c.808_810del	XP_011527516.1:p.Ile270del
XM_017027796.1:c.337_339del	XP_016883285.1:p.Ile113del
XR_002958465.1:n.818_820del
XR_002958466.1:n.938_940del
XR_002958467.1:n.497_499del
NM_001042472.3:c.808_810del MANE Select	NP_001035937.1:p.Ile270del
NM_015600.5:c.808_810del	NP_056415.1:p.Ile270del