Canonical Allele Identifier: CA2243487183

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2665202_2665215delinsGTTCTGGAGGCTTT , CM000679.2:g.2665202_2665215delinsGTTCTGGAGGCTTT	GRCh38
NC_000017.10:g.2568496_2568509delinsGTTCTGGAGGCTTT , CM000679.1:g.2568496_2568509delinsGTTCTGGAGGCTTT	GRCh37
NC_000017.9:g.2515246_2515259delinsGTTCTGGAGGCTTT	NCBI36
NG_009799.1:g.76574_76587delinsGTTCTGGAGGCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.33-170_33-157delinsGTTCTGGAGGCTTT MANE Select	ENSP00000380378.4:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000674608.1:c.87-170_87-157delinsGTTCTGGAGGCTTT	ENSP00000501976.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
ENST00000674717.1:c.-3-1790_-3-1777delinsGTTCTGGAGGCTTT	ENSP00000501931.1:n.-3-1790_-3-1777delinsGTTCTGGAGGCTTT
ENST00000675202.1:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000502843.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000675331.1:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000502031.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000675390.1:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000501969.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000675430.1:n.260-170_260-157delinsGTTCTGGAGGCTTT
ENST00000675621.1:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000502117.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000675764.1:c.131-170_131-157delinsGTTCTGGAGGCTTT	ENSP00000502242.1:n.131-170_131-157delinsGTTCTGGAGGCTTT
ENST00000676077.1:c.-163-170_-163-157delinsGTTCTGGAGGCTTT	ENSP00000502507.1:n.-163-170_-163-157delinsGTTCTGGAGGCTTT
ENST00000676098.1:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000502735.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000676188.1:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000502577.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000676201.1:n.272-814_272-801delinsGTTCTGGAGGCTTT
ENST00000676353.1:c.-78-814_-78-801delinsGTTCTGGAGGCTTT	ENSP00000502737.1:n.-78-814_-78-801delinsGTTCTGGAGGCTTT
ENST00000676456.1:n.223-814_223-801delinsGTTCTGGAGGCTTT
ENST00000397195.9:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000380378.4:n.33-170_33-157delinsGTTCTGGAGGCTTT
ENST00000570400.1:c.33-814_33-801delinsGTTCTGGAGGCTTT	ENSP00000460258.1:n.33-814_33-801delinsGTTCTGGAGGCTTT
ENST00000572915.6:n.273-1790_273-1777delinsGTTCTGGAGGCTTT
ENST00000574816.5:n.31-11112_31-11099delinsGTTCTGGAGGCTTT
ENST00000575477.5:n.620-814_620-801delinsGTTCTGGAGGCTTT
ENST00000576586.5:c.33-170_33-157delinsGTTCTGGAGGCTTT	ENSP00000461087.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
NM_000430.3:c.33-170_33-157delinsGTTCTGGAGGCTTT	NP_000421.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
XM_011523901.1:c.87-170_87-157delinsGTTCTGGAGGCTTT	XP_011522203.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
XM_011523902.1:c.87-170_87-157delinsGTTCTGGAGGCTTT	XP_011522204.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
XM_011523903.1:c.87-170_87-157delinsGTTCTGGAGGCTTT	XP_011522205.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
XM_011523904.1:c.87-170_87-157delinsGTTCTGGAGGCTTT	XP_011522206.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
XM_011523901.2:c.87-170_87-157delinsGTTCTGGAGGCTTT	XP_011522203.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
XM_011523902.3:c.87-170_87-157delinsGTTCTGGAGGCTTT	XP_011522204.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
XM_011523903.2:c.87-170_87-157delinsGTTCTGGAGGCTTT	XP_011522205.1:n.87-170_87-157delinsGTTCTGGAGGCTTT
XM_017024701.1:c.33-170_33-157delinsGTTCTGGAGGCTTT	XP_016880190.1:n.33-170_33-157delinsGTTCTGGAGGCTTT
XM_017024702.2:c.-78-814_-78-801delinsGTTCTGGAGGCTTT	XP_016880191.1:n.-78-814_-78-801delinsGTTCTGGAGGCTTT
NM_000430.4:c.33-170_33-157delinsGTTCTGGAGGCTTT MANE Select	NP_000421.1:n.33-170_33-157delinsGTTCTGGAGGCTTT