Canonical Allele Identifier: CA408455879

Gene: ABHD12

Linked Data

• MyVariant Identifiers: chr20:g.25288639T>G (hg19) ; chr20:g.25308003T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25308003T>G , CM000682.2:g.25308003T>G	GRCh38
NC_000020.10:g.25288639T>G , CM000682.1:g.25288639T>G	GRCh37
NC_000020.9:g.25236639T>G	NCBI36
NG_028119.1:g.87980A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339157.10:c.830A>C MANE Select	ENSP00000341408.5:p.Asn277Thr
ENST00000376542.8:c.830A>C	ENSP00000365725.3:p.Asn277Thr
ENST00000465694.2:c.284A>C	ENSP00000459278.2:p.Asn95Thr
ENST00000671784.1:c.284A>C	ENSP00000500451.1:p.Asn95Thr
ENST00000671858.1:c.284A>C	ENSP00000500550.1:p.Asn95Thr
ENST00000672001.1:n.341A>C
ENST00000672114.1:c.284A>C	ENSP00000499945.1:p.Asn95Thr
ENST00000672258.1:c.284A>C	ENSP00000499868.1:p.Asn95Thr
ENST00000672331.1:c.284A>C	ENSP00000500286.1:p.Asn95Thr
ENST00000672358.1:c.284A>C	ENSP00000500062.1:p.Asn95Thr
ENST00000672406.1:c.*169A>C	ENSP00000500208.1:n.*169A>C
ENST00000672566.1:c.359A>C	ENSP00000500106.1:p.Asn120Thr
ENST00000672596.1:c.284A>C	ENSP00000500290.1:p.Asn95Thr
ENST00000672871.1:c.284A>C	ENSP00000499949.1:p.Asn95Thr
ENST00000673094.1:c.284A>C	ENSP00000500257.1:p.Asn95Thr
ENST00000673121.1:c.386A>C	ENSP00000499839.1:p.Asn129Thr
ENST00000673227.1:c.284A>C	ENSP00000500514.1:p.Asn95Thr
ENST00000673524.1:c.392A>C
ENST00000339157.9:c.830A>C	ENSP00000341408.5:p.Asn277Thr
ENST00000376542.7:c.830A>C	ENSP00000365725.3:p.Asn277Thr
ENST00000481556.1:n.484A>C
ENST00000491682.5:c.359A>C	ENSP00000459495.1:p.Asn120Thr
ENST00000576316.5:c.134A>C	ENSP00000459121.1:p.Asn45Thr
NM_001042472.2:c.830A>C	NP_001035937.1:p.Asn277Thr
NM_015600.4:c.830A>C	NP_056415.1:p.Asn277Thr
XM_005260698.1:c.830A>C	XP_005260755.1:p.Asn277Thr
XM_005260699.3:c.830A>C	XP_005260756.1:p.Asn277Thr
XM_005260700.1:c.359A>C	XP_005260757.1:p.Asn120Thr
XM_011529214.1:c.830A>C	XP_011527516.1:p.Asn277Thr
XM_011529215.1:c.359A>C	XP_011527517.1:p.Asn120Thr
XM_011529216.1:c.359A>C	XP_011527518.1:p.Asn120Thr
XM_011529217.1:c.173A>C	XP_011527519.1:p.Asn58Thr
XM_011529218.1:c.173A>C	XP_011527520.1:p.Asn58Thr
XM_011529214.2:c.830A>C	XP_011527516.1:p.Asn277Thr
XM_017027796.1:c.359A>C	XP_016883285.1:p.Asn120Thr
XR_002958465.1:n.840A>C
XR_002958466.1:n.960A>C
XR_002958467.1:n.519A>C
NM_001042472.3:c.830A>C MANE Select	NP_001035937.1:p.Asn277Thr
NM_015600.5:c.830A>C	NP_056415.1:p.Asn277Thr