Canonical Allele Identifier: CA408455846

Gene: ABHD12

Linked Data

• MyVariant Identifiers: chr20:g.25288624G>A (hg19) ; chr20:g.25307988G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.25307988G>A , CM000682.2:g.25307988G>A	GRCh38
NC_000020.10:g.25288624G>A , CM000682.1:g.25288624G>A	GRCh37
NC_000020.9:g.25236624G>A	NCBI36
NG_028119.1:g.87995C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339157.10:c.845C>T MANE Select	ENSP00000341408.5:p.Ala282Val
ENST00000376542.8:c.845C>T	ENSP00000365725.3:p.Ala282Val
ENST00000465694.2:c.299C>T	ENSP00000459278.2:p.Ala100Val
ENST00000671784.1:c.299C>T	ENSP00000500451.1:p.Ala100Val
ENST00000671858.1:c.299C>T	ENSP00000500550.1:p.Ala100Val
ENST00000672001.1:n.356C>T
ENST00000672114.1:c.299C>T	ENSP00000499945.1:p.Ala100Val
ENST00000672258.1:c.299C>T	ENSP00000499868.1:p.Ala100Val
ENST00000672331.1:c.299C>T	ENSP00000500286.1:p.Ala100Val
ENST00000672358.1:c.299C>T	ENSP00000500062.1:p.Ala100Val
ENST00000672406.1:c.*184C>T	ENSP00000500208.1:n.*184C>T
ENST00000672566.1:c.374C>T	ENSP00000500106.1:p.Ala125Val
ENST00000672596.1:c.299C>T	ENSP00000500290.1:p.Ala100Val
ENST00000672871.1:c.299C>T	ENSP00000499949.1:p.Ala100Val
ENST00000673094.1:c.299C>T	ENSP00000500257.1:p.Ala100Val
ENST00000673121.1:c.401C>T	ENSP00000499839.1:p.Ala134Val
ENST00000673227.1:c.299C>T	ENSP00000500514.1:p.Ala100Val
ENST00000673524.1:c.407C>T
ENST00000339157.9:c.845C>T	ENSP00000341408.5:p.Ala282Val
ENST00000376542.7:c.845C>T	ENSP00000365725.3:p.Ala282Val
ENST00000481556.1:n.499C>T
ENST00000491682.5:c.374C>T	ENSP00000459495.1:p.Ala125Val
ENST00000576316.5:c.149C>T	ENSP00000459121.1:p.Ala50Val
NM_001042472.2:c.845C>T	NP_001035937.1:p.Ala282Val
NM_015600.4:c.845C>T	NP_056415.1:p.Ala282Val
XM_005260698.1:c.845C>T	XP_005260755.1:p.Ala282Val
XM_005260699.3:c.845C>T	XP_005260756.1:p.Ala282Val
XM_005260700.1:c.374C>T	XP_005260757.1:p.Ala125Val
XM_011529214.1:c.845C>T	XP_011527516.1:p.Ala282Val
XM_011529215.1:c.374C>T	XP_011527517.1:p.Ala125Val
XM_011529216.1:c.374C>T	XP_011527518.1:p.Ala125Val
XM_011529217.1:c.188C>T	XP_011527519.1:p.Ala63Val
XM_011529218.1:c.188C>T	XP_011527520.1:p.Ala63Val
XM_011529214.2:c.845C>T	XP_011527516.1:p.Ala282Val
XM_017027796.1:c.374C>T	XP_016883285.1:p.Ala125Val
XR_002958465.1:n.855C>T
XR_002958466.1:n.975C>T
XR_002958467.1:n.534C>T
NM_001042472.3:c.845C>T MANE Select	NP_001035937.1:p.Ala282Val
NM_015600.5:c.845C>T	NP_056415.1:p.Ala282Val