Canonical Allele Identifier: CA2243487566

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2665983_2665986delinsATTT , CM000679.2:g.2665983_2665986delinsATTT	GRCh38
NC_000017.10:g.2569277_2569280delinsATTT , CM000679.1:g.2569277_2569280delinsATTT	GRCh37
NC_000017.9:g.2516027_2516030delinsATTT	NCBI36
NG_009799.1:g.77355_77358delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.118-33_118-30delinsATTT MANE Select	ENSP00000380378.4:n.118-33_118-30delinsATTT
ENST00000674608.1:c.172-33_172-30delinsATTT	ENSP00000501976.1:n.172-33_172-30delinsATTT
ENST00000674717.1:c.-3-1009_-3-1006delinsATTT	ENSP00000501931.1:n.-3-1009_-3-1006delinsATTT
ENST00000675202.1:c.118-33_118-30delinsATTT	ENSP00000502843.1:n.118-33_118-30delinsATTT
ENST00000675331.1:c.118-33_118-30delinsATTT	ENSP00000502031.1:n.118-33_118-30delinsATTT
ENST00000675390.1:c.118-33_118-30delinsATTT	ENSP00000501969.1:n.118-33_118-30delinsATTT
ENST00000675430.1:n.345-33_345-30delinsATTT
ENST00000675621.1:c.118-33_118-30delinsATTT	ENSP00000502117.1:n.118-33_118-30delinsATTT
ENST00000675764.1:c.*72-33_*72-30delinsATTT	ENSP00000502242.1:n.*72-33_*72-30delinsATTT
ENST00000676077.1:c.-78-33_-78-30delinsATTT	ENSP00000502507.1:n.-78-33_-78-30delinsATTT
ENST00000676098.1:c.118-33_118-30delinsATTT	ENSP00000502735.1:n.118-33_118-30delinsATTT
ENST00000676188.1:c.118-33_118-30delinsATTT	ENSP00000502577.1:n.118-33_118-30delinsATTT
ENST00000676201.1:n.272-33_272-30delinsATTT
ENST00000676353.1:c.-78-33_-78-30delinsATTT	ENSP00000502737.1:n.-78-33_-78-30delinsATTT
ENST00000676456.1:n.223-33_223-30delinsATTT
ENST00000397195.9:c.118-33_118-30delinsATTT	ENSP00000380378.4:n.118-33_118-30delinsATTT
ENST00000570400.1:c.33-33_33-30delinsATTT	ENSP00000460258.1:n.33-33_33-30delinsATTT
ENST00000572915.6:n.273-1009_273-1006delinsATTT
ENST00000574816.5:n.31-10331_31-10328delinsATTT
ENST00000575477.5:n.620-33_620-30delinsATTT
ENST00000576586.5:c.118-33_118-30delinsATTT	ENSP00000461087.1:n.118-33_118-30delinsATTT
ENST00000609078.1:n.77-33_77-30delinsATTT
NM_000430.3:c.118-33_118-30delinsATTT	NP_000421.1:n.118-33_118-30delinsATTT
XM_011523901.1:c.172-33_172-30delinsATTT	XP_011522203.1:n.172-33_172-30delinsATTT
XM_011523902.1:c.172-33_172-30delinsATTT	XP_011522204.1:n.172-33_172-30delinsATTT
XM_011523903.1:c.172-33_172-30delinsATTT	XP_011522205.1:n.172-33_172-30delinsATTT
XM_011523904.1:c.172-33_172-30delinsATTT	XP_011522206.1:n.172-33_172-30delinsATTT
XM_011523901.2:c.172-33_172-30delinsATTT	XP_011522203.1:n.172-33_172-30delinsATTT
XM_011523902.3:c.172-33_172-30delinsATTT	XP_011522204.1:n.172-33_172-30delinsATTT
XM_011523903.2:c.172-33_172-30delinsATTT	XP_011522205.1:n.172-33_172-30delinsATTT
XM_017024701.1:c.118-33_118-30delinsATTT	XP_016880190.1:n.118-33_118-30delinsATTT
XM_017024702.2:c.-78-33_-78-30delinsATTT	XP_016880191.1:n.-78-33_-78-30delinsATTT
NM_000430.4:c.118-33_118-30delinsATTT MANE Select	NP_000421.1:n.118-33_118-30delinsATTT