Canonical Allele Identifier: CA9795968

Gene: ABHD12

Linked Data

• ClinVar Variation Id: 1354285
• ClinVar RCV Id: RCV001887772
• dbSNP Id: rs775417181
• ExAC: 20:25288643 T / C
• gnomAD v2: 20-25288643-T-C
• gnomAD v3: 20-25308007-T-C
• gnomAD v4: 20-25308007-T-C
• MyVariant Identifiers: chr20:g.25288643T>C (hg19) ; chr20:g.25308007T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25308007T>C , CM000682.2:g.25308007T>C	GRCh38
NC_000020.10:g.25288643T>C , CM000682.1:g.25288643T>C	GRCh37
NC_000020.9:g.25236643T>C	NCBI36
NG_028119.1:g.87976A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339157.10:c.826A>G MANE Select	ENSP00000341408.5:p.Thr276Ala
ENST00000376542.8:c.826A>G	ENSP00000365725.3:p.Thr276Ala
ENST00000465694.2:c.280A>G	ENSP00000459278.2:p.Thr94Ala
ENST00000671784.1:c.280A>G	ENSP00000500451.1:p.Thr94Ala
ENST00000671858.1:c.280A>G	ENSP00000500550.1:p.Thr94Ala
ENST00000672001.1:n.337A>G
ENST00000672114.1:c.280A>G	ENSP00000499945.1:p.Thr94Ala
ENST00000672258.1:c.280A>G	ENSP00000499868.1:p.Thr94Ala
ENST00000672331.1:c.280A>G	ENSP00000500286.1:p.Thr94Ala
ENST00000672358.1:c.280A>G	ENSP00000500062.1:p.Thr94Ala
ENST00000672406.1:c.*165A>G	ENSP00000500208.1:n.*165A>G
ENST00000672566.1:c.355A>G	ENSP00000500106.1:p.Thr119Ala
ENST00000672596.1:c.280A>G	ENSP00000500290.1:p.Thr94Ala
ENST00000672871.1:c.280A>G	ENSP00000499949.1:p.Thr94Ala
ENST00000673094.1:c.280A>G	ENSP00000500257.1:p.Thr94Ala
ENST00000673121.1:c.382A>G	ENSP00000499839.1:p.Thr128Ala
ENST00000673227.1:c.280A>G	ENSP00000500514.1:p.Thr94Ala
ENST00000673524.1:c.388A>G
ENST00000339157.9:c.826A>G	ENSP00000341408.5:p.Thr276Ala
ENST00000376542.7:c.826A>G	ENSP00000365725.3:p.Thr276Ala
ENST00000481556.1:n.480A>G
ENST00000491682.5:c.355A>G	ENSP00000459495.1:p.Thr119Ala
ENST00000576316.5:c.130A>G	ENSP00000459121.1:p.Thr44Ala
NM_001042472.2:c.826A>G	NP_001035937.1:p.Thr276Ala
NM_015600.4:c.826A>G	NP_056415.1:p.Thr276Ala
XM_005260698.1:c.826A>G	XP_005260755.1:p.Thr276Ala
XM_005260699.3:c.826A>G	XP_005260756.1:p.Thr276Ala
XM_005260700.1:c.355A>G	XP_005260757.1:p.Thr119Ala
XM_011529214.1:c.826A>G	XP_011527516.1:p.Thr276Ala
XM_011529215.1:c.355A>G	XP_011527517.1:p.Thr119Ala
XM_011529216.1:c.355A>G	XP_011527518.1:p.Thr119Ala
XM_011529217.1:c.169A>G	XP_011527519.1:p.Thr57Ala
XM_011529218.1:c.169A>G	XP_011527520.1:p.Thr57Ala
XM_011529214.2:c.826A>G	XP_011527516.1:p.Thr276Ala
XM_017027796.1:c.355A>G	XP_016883285.1:p.Thr119Ala
XR_002958465.1:n.836A>G
XR_002958466.1:n.956A>G
XR_002958467.1:n.515A>G
NM_001042472.3:c.826A>G MANE Select	NP_001035937.1:p.Thr276Ala
NM_015600.5:c.826A>G	NP_056415.1:p.Thr276Ala