Canonical Allele Identifier: CA2243487594
Gene: PAFAH1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2666052_2666053delinsGA , CM000679.2:g.2666052_2666053delinsGA GRCh38
NC_000017.10:g.2569346_2569347delinsGA , CM000679.1:g.2569346_2569347delinsGA GRCh37
NC_000017.9:g.2516096_2516097delinsGA NCBI36
NG_009799.1:g.77424_77425delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.154_155delinsGA MANE Select ENSP00000380378.4:p.Glu52=
ENST00000674608.1:c.208_209delinsGA ENSP00000501976.1:p.Glu70=
ENST00000674717.1:c.-3-940_-3-939delinsGA ENSP00000501931.1:n.-3-940_-3-939delinsGA
ENST00000675202.1:c.154_155delinsGA ENSP00000502843.1:p.Glu52=
ENST00000675331.1:c.154_155delinsGA ENSP00000502031.1:p.Glu52=
ENST00000675390.1:c.154_155delinsGA ENSP00000501969.1:p.Glu52=
ENST00000675430.1:n.381_382delinsGA
ENST00000675621.1:c.154_155delinsGA ENSP00000502117.1:p.Glu52=
ENST00000675764.1:c.*108_*109delinsGA ENSP00000502242.1:n.*108_*109delinsGA
ENST00000676077.1:c.-42_-41delinsGA ENSP00000502507.1:n.-42_-41delinsGA
ENST00000676098.1:c.154_155delinsGA ENSP00000502735.1:p.Glu52=
ENST00000676188.1:c.154_155delinsGA ENSP00000502577.1:p.Glu52=
ENST00000676201.1:n.308_309delinsGA
ENST00000676353.1:c.-42_-41delinsGA ENSP00000502737.1:n.-42_-41delinsGA
ENST00000676456.1:n.259_260delinsGA
ENST00000397195.9:c.154_155delinsGA ENSP00000380378.4:p.Glu52=
ENST00000570400.1:c.*24_*25delinsGA ENSP00000460258.1:n.*24_*25delinsGA
ENST00000572915.6:n.273-940_273-939delinsGA
ENST00000574816.5:n.31-10262_31-10261delinsGA
ENST00000575477.5:n.656_657delinsGA
ENST00000576586.5:c.154_155delinsGA ENSP00000461087.1:p.Glu52=
ENST00000609078.1:n.113_114delinsGA
NM_000430.3:c.154_155delinsGA NP_000421.1:p.Glu52=
XM_011523901.1:c.208_209delinsGA XP_011522203.1:p.Glu70=
XM_011523902.1:c.208_209delinsGA XP_011522204.1:p.Glu70=
XM_011523903.1:c.208_209delinsGA XP_011522205.1:p.Glu70=
XM_011523904.1:c.208_209delinsGA XP_011522206.1:p.Glu70=
XM_011523901.2:c.208_209delinsGA XP_011522203.1:p.Glu70=
XM_011523902.3:c.208_209delinsGA XP_011522204.1:p.Glu70=
XM_011523903.2:c.208_209delinsGA XP_011522205.1:p.Glu70=
XM_017024701.1:c.154_155delinsGA XP_016880190.1:p.Glu52=
XM_017024702.2:c.-42_-41delinsGA XP_016880191.1:n.-42_-41delinsGA
NM_000430.4:c.154_155delinsGA MANE Select NP_000421.1:p.Glu52=