Canonical Allele Identifier: CA2243490646

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2672568_2672581delinsCCCCATGGTAAAAT , CM000679.2:g.2672568_2672581delinsCCCCATGGTAAAAT	GRCh38
NC_000017.10:g.2575862_2575875delinsCCCCATGGTAAAAT , CM000679.1:g.2575862_2575875delinsCCCCATGGTAAAAT	GRCh37
NC_000017.9:g.2522612_2522625delinsCCCCATGGTAAAAT	NCBI36
NG_009799.1:g.83940_83953delinsCCCCATGGTAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.569-87_569-74delinsCCCCATGGTAAAAT MANE Select	ENSP00000380378.4:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000571495.2:n.265_278delinsCCCCATGGTAAAAT
ENST00000674608.1:c.623-87_623-74delinsCCCCATGGTAAAAT	ENSP00000501976.1:n.623-87_623-74delinsCCCCATGGTAAAAT
ENST00000674717.1:c.374-87_374-74delinsCCCCATGGTAAAAT	ENSP00000501931.1:n.374-87_374-74delinsCCCCATGGTAAAAT
ENST00000675202.1:c.569-87_569-74delinsCCCCATGGTAAAAT	ENSP00000502843.1:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000675331.1:c.569-87_569-74delinsCCCCATGGTAAAAT	ENSP00000502031.1:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000675390.1:c.569-87_569-74delinsCCCCATGGTAAAAT	ENSP00000501969.1:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000675574.1:n.252_265delinsCCCCATGGTAAAAT
ENST00000675621.1:c.569-87_569-74delinsCCCCATGGTAAAAT	ENSP00000502117.1:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000675764.1:c.*523-87_*523-74delinsCCCCATGGTAAAAT	ENSP00000502242.1:n.*523-87_*523-74delinsCCCCATGGTAAAAT
ENST00000676077.1:c.374-1492_374-1479delinsCCCCATGGTAAAAT	ENSP00000502507.1:n.374-1492_374-1479delinsCCCCATGGTAAAAT
ENST00000676098.1:c.569-87_569-74delinsCCCCATGGTAAAAT	ENSP00000502735.1:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000676188.1:c.569-87_569-74delinsCCCCATGGTAAAAT	ENSP00000502577.1:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000676353.1:c.374-87_374-74delinsCCCCATGGTAAAAT	ENSP00000502737.1:n.374-87_374-74delinsCCCCATGGTAAAAT
ENST00000397193.7:n.377-87_377-74delinsCCCCATGGTAAAAT
ENST00000397195.9:c.569-87_569-74delinsCCCCATGGTAAAAT	ENSP00000380378.4:n.569-87_569-74delinsCCCCATGGTAAAAT
ENST00000572915.6:n.537-87_537-74delinsCCCCATGGTAAAAT
ENST00000574468.1:c.65-87_65-74delinsCCCCATGGTAAAAT	ENSP00000460591.1:n.65-87_65-74delinsCCCCATGGTAAAAT
ENST00000574816.5:n.31-3746_31-3733delinsCCCCATGGTAAAAT
NM_000430.3:c.569-87_569-74delinsCCCCATGGTAAAAT	NP_000421.1:n.569-87_569-74delinsCCCCATGGTAAAAT
XM_011523901.1:c.623-87_623-74delinsCCCCATGGTAAAAT	XP_011522203.1:n.623-87_623-74delinsCCCCATGGTAAAAT
XM_011523902.1:c.623-87_623-74delinsCCCCATGGTAAAAT	XP_011522204.1:n.623-87_623-74delinsCCCCATGGTAAAAT
XM_011523903.1:c.623-87_623-74delinsCCCCATGGTAAAAT	XP_011522205.1:n.623-87_623-74delinsCCCCATGGTAAAAT
XM_011523904.1:c.623-1492_623-1479delinsCCCCATGGTAAAAT	XP_011522206.1:n.623-1492_623-1479delinsCCCCATGGTAAAAT
XM_011523901.2:c.623-87_623-74delinsCCCCATGGTAAAAT	XP_011522203.1:n.623-87_623-74delinsCCCCATGGTAAAAT
XM_011523902.3:c.623-87_623-74delinsCCCCATGGTAAAAT	XP_011522204.1:n.623-87_623-74delinsCCCCATGGTAAAAT
XM_011523903.2:c.623-87_623-74delinsCCCCATGGTAAAAT	XP_011522205.1:n.623-87_623-74delinsCCCCATGGTAAAAT
XM_017024701.1:c.569-87_569-74delinsCCCCATGGTAAAAT	XP_016880190.1:n.569-87_569-74delinsCCCCATGGTAAAAT
XM_017024702.2:c.374-87_374-74delinsCCCCATGGTAAAAT	XP_016880191.1:n.374-87_374-74delinsCCCCATGGTAAAAT
NM_000430.4:c.569-87_569-74delinsCCCCATGGTAAAAT MANE Select	NP_000421.1:n.569-87_569-74delinsCCCCATGGTAAAAT