Canonical Allele Identifier: CA2243487612

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2666101_2666103delinsCTT , CM000679.2:g.2666101_2666103delinsCTT	GRCh38
NC_000017.10:g.2569395_2569397delinsCTT , CM000679.1:g.2569395_2569397delinsCTT	GRCh37
NC_000017.9:g.2516145_2516147delinsCTT	NCBI36
NG_009799.1:g.77473_77475delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.192+11_192+13delinsCTT MANE Select	ENSP00000380378.4:n.192+11_192+13delinsCTT
ENST00000674608.1:c.246+11_246+13delinsCTT	ENSP00000501976.1:n.246+11_246+13delinsCTT
ENST00000674717.1:c.-3-891_-3-889delinsCTT	ENSP00000501931.1:n.-3-891_-3-889delinsCTT
ENST00000675202.1:c.192+11_192+13delinsCTT	ENSP00000502843.1:n.192+11_192+13delinsCTT
ENST00000675331.1:c.192+11_192+13delinsCTT	ENSP00000502031.1:n.192+11_192+13delinsCTT
ENST00000675390.1:c.192+11_192+13delinsCTT	ENSP00000501969.1:n.192+11_192+13delinsCTT
ENST00000675430.1:n.419+11_419+13delinsCTT
ENST00000675621.1:c.192+11_192+13delinsCTT	ENSP00000502117.1:n.192+11_192+13delinsCTT
ENST00000675764.1:c.*146+11_*146+13delinsCTT	ENSP00000502242.1:n.*146+11_*146+13delinsCTT
ENST00000676077.1:c.-4+11_-4+13delinsCTT	ENSP00000502507.1:n.-4+11_-4+13delinsCTT
ENST00000676098.1:c.192+11_192+13delinsCTT	ENSP00000502735.1:n.192+11_192+13delinsCTT
ENST00000676188.1:c.192+11_192+13delinsCTT	ENSP00000502577.1:n.192+11_192+13delinsCTT
ENST00000676201.1:n.346+11_346+13delinsCTT
ENST00000676353.1:c.-4+11_-4+13delinsCTT	ENSP00000502737.1:n.-4+11_-4+13delinsCTT
ENST00000676456.1:n.297+11_297+13delinsCTT
ENST00000397195.9:c.192+11_192+13delinsCTT	ENSP00000380378.4:n.192+11_192+13delinsCTT
ENST00000570400.1:c.*62+11_*62+13delinsCTT	ENSP00000460258.1:n.*62+11_*62+13delinsCTT
ENST00000572915.6:n.273-891_273-889delinsCTT
ENST00000574816.5:n.31-10213_31-10211delinsCTT
ENST00000576586.5:c.192+11_192+13delinsCTT	ENSP00000461087.1:n.192+11_192+13delinsCTT
ENST00000609078.1:n.151+11_151+13delinsCTT
NM_000430.3:c.192+11_192+13delinsCTT	NP_000421.1:n.192+11_192+13delinsCTT
XM_011523901.1:c.246+11_246+13delinsCTT	XP_011522203.1:n.246+11_246+13delinsCTT
XM_011523902.1:c.246+11_246+13delinsCTT	XP_011522204.1:n.246+11_246+13delinsCTT
XM_011523903.1:c.246+11_246+13delinsCTT	XP_011522205.1:n.246+11_246+13delinsCTT
XM_011523904.1:c.246+11_246+13delinsCTT	XP_011522206.1:n.246+11_246+13delinsCTT
XM_011523901.2:c.246+11_246+13delinsCTT	XP_011522203.1:n.246+11_246+13delinsCTT
XM_011523902.3:c.246+11_246+13delinsCTT	XP_011522204.1:n.246+11_246+13delinsCTT
XM_011523903.2:c.246+11_246+13delinsCTT	XP_011522205.1:n.246+11_246+13delinsCTT
XM_017024701.1:c.192+11_192+13delinsCTT	XP_016880190.1:n.192+11_192+13delinsCTT
XM_017024702.2:c.-4+11_-4+13delinsCTT	XP_016880191.1:n.-4+11_-4+13delinsCTT
NM_000430.4:c.192+11_192+13delinsCTT MANE Select	NP_000421.1:n.192+11_192+13delinsCTT