Canonical Allele Identifier: CA2652223797

Gene: ABHD12

Linked Data

• gnomAD v4: 20-25307861-TTAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25307865_25307868del , CM000682.2:g.25307865_25307868del	GRCh38
NC_000020.10:g.25288501_25288504del , CM000682.1:g.25288501_25288504del	GRCh37
NC_000020.9:g.25236501_25236504del	NCBI36
NG_028119.1:g.88118_88121del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339157.10:c.867+101_867+104del MANE Select	ENSP00000341408.5:n.867+101_867+104del
ENST00000376542.8:c.867+101_867+104del	ENSP00000365725.3:n.867+101_867+104del
ENST00000465694.2:c.321+101_321+104del	ENSP00000459278.2:n.321+101_321+104del
ENST00000671784.1:c.321+101_321+104del	ENSP00000500451.1:n.321+101_321+104del
ENST00000671858.1:c.321+101_321+104del	ENSP00000500550.1:n.321+101_321+104del
ENST00000672001.1:n.378+101_378+104del
ENST00000672114.1:c.321+101_321+104del	ENSP00000499945.1:n.321+101_321+104del
ENST00000672258.1:c.321+101_321+104del	ENSP00000499868.1:n.321+101_321+104del
ENST00000672331.1:c.321+101_321+104del	ENSP00000500286.1:n.321+101_321+104del
ENST00000672358.1:c.321+101_321+104del	ENSP00000500062.1:n.321+101_321+104del
ENST00000672406.1:c.*206+101_*206+104del	ENSP00000500208.1:n.*206+101_*206+104del
ENST00000672566.1:c.396+101_396+104del	ENSP00000500106.1:n.396+101_396+104del
ENST00000672596.1:c.321+101_321+104del	ENSP00000500290.1:n.321+101_321+104del
ENST00000672871.1:c.321+101_321+104del	ENSP00000499949.1:n.321+101_321+104del
ENST00000673094.1:c.321+101_321+104del	ENSP00000500257.1:n.321+101_321+104del
ENST00000673121.1:c.423+101_423+104del	ENSP00000499839.1:n.423+101_423+104del
ENST00000673227.1:c.321+101_321+104del	ENSP00000500514.1:n.321+101_321+104del
ENST00000673524.1:c.429+101_429+104del
ENST00000339157.9:c.867+101_867+104del	ENSP00000341408.5:n.867+101_867+104del
ENST00000376542.7:c.867+101_867+104del	ENSP00000365725.3:n.867+101_867+104del
ENST00000481556.1:n.521+101_521+104del
ENST00000491682.5:c.396+101_396+104del	ENSP00000459495.1:n.396+101_396+104del
ENST00000576316.5:c.171+101_171+104del	ENSP00000459121.1:n.171+101_171+104del
NM_001042472.2:c.867+101_867+104del	NP_001035937.1:n.867+101_867+104del
NM_015600.4:c.867+101_867+104del	NP_056415.1:n.867+101_867+104del
XM_005260698.1:c.867+101_867+104del	XP_005260755.1:n.867+101_867+104del
XM_005260699.3:c.867+101_867+104del	XP_005260756.1:n.867+101_867+104del
XM_005260700.1:c.396+101_396+104del	XP_005260757.1:n.396+101_396+104del
XM_011529214.1:c.867+101_867+104del	XP_011527516.1:n.867+101_867+104del
XM_011529215.1:c.396+101_396+104del	XP_011527517.1:n.396+101_396+104del
XM_011529216.1:c.396+101_396+104del	XP_011527518.1:n.396+101_396+104del
XM_011529217.1:c.210+101_210+104del	XP_011527519.1:n.210+101_210+104del
XM_011529218.1:c.210+101_210+104del	XP_011527520.1:n.210+101_210+104del
XM_011529214.2:c.867+101_867+104del	XP_011527516.1:n.867+101_867+104del
XM_017027796.1:c.396+101_396+104del	XP_016883285.1:n.396+101_396+104del
XR_002958465.1:n.877+101_877+104del
XR_002958466.1:n.997+101_997+104del
XR_002958467.1:n.556+101_556+104del
NM_001042472.3:c.867+101_867+104del MANE Select	NP_001035937.1:n.867+101_867+104del
NM_015600.5:c.867+101_867+104del	NP_056415.1:n.867+101_867+104del