Canonical Allele Identifier: CA272387

Gene: PAFAH1B1

Linked Data

• ClinVar Variation Id: 159506
• ClinVar RCV Id: RCV000147022 ; RCV002515970
• dbSNP Id: rs587784253
• gnomAD v4: 17-2666046-CT-C
• MyVariant Identifiers: chr17:g.2569344del (hg19) ; chr17:g.2666050del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2666050del , CM000679.2:g.2666050del	GRCh38
NC_000017.10:g.2569344del , CM000679.1:g.2569344del	GRCh37
NC_000017.9:g.2516094del	NCBI36
NG_009799.1:g.77422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.152del MANE Select	ENSP00000380378.4:p.Leu51TrpfsTer18
ENST00000674608.1:c.206del	ENSP00000501976.1:p.Leu69TrpfsTer18
ENST00000674717.1:c.-3-942del	ENSP00000501931.1:n.-3-942del
ENST00000675202.1:c.152del	ENSP00000502843.1:p.Leu51TrpfsTer18
ENST00000675331.1:c.152del	ENSP00000502031.1:p.Leu51TrpfsTer18
ENST00000675390.1:c.152del	ENSP00000501969.1:p.Leu51TrpfsTer18
ENST00000675430.1:n.379del
ENST00000675621.1:c.152del	ENSP00000502117.1:p.Leu51TrpfsTer18
ENST00000675764.1:c.*106del	ENSP00000502242.1:n.*106del
ENST00000676077.1:c.-44del	ENSP00000502507.1:n.-44del
ENST00000676098.1:c.152del	ENSP00000502735.1:p.Leu51TrpfsTer18
ENST00000676188.1:c.152del	ENSP00000502577.1:p.Leu51TrpfsTer18
ENST00000676201.1:n.306del
ENST00000676353.1:c.-44del	ENSP00000502737.1:n.-44del
ENST00000676456.1:n.257del
ENST00000397195.9:c.152del	ENSP00000380378.4:p.Leu51TrpfsTer18
ENST00000570400.1:c.*22del	ENSP00000460258.1:n.*22del
ENST00000572915.6:n.273-942del
ENST00000574816.5:n.31-10264del
ENST00000575477.5:n.654del
ENST00000576586.5:c.152del	ENSP00000461087.1:p.Leu51TrpfsTer18
ENST00000609078.1:n.111del
NM_000430.3:c.152del	NP_000421.1:p.Leu51TrpfsTer18
XM_011523901.1:c.206del	XP_011522203.1:p.Leu69TrpfsTer18
XM_011523902.1:c.206del	XP_011522204.1:p.Leu69TrpfsTer18
XM_011523903.1:c.206del	XP_011522205.1:p.Leu69TrpfsTer18
XM_011523904.1:c.206del	XP_011522206.1:p.Leu69TrpfsTer18
XM_011523901.2:c.206del	XP_011522203.1:p.Leu69TrpfsTer18
XM_011523902.3:c.206del	XP_011522204.1:p.Leu69TrpfsTer18
XM_011523903.2:c.206del	XP_011522205.1:p.Leu69TrpfsTer18
XM_017024701.1:c.152del	XP_016880190.1:p.Leu51TrpfsTer18
XM_017024702.2:c.-44del	XP_016880191.1:n.-44del
NM_000430.4:c.152del MANE Select	NP_000421.1:p.Leu51TrpfsTer18