Canonical Allele Identifier: CA8283131

Gene: PAFAH1B1

Linked Data

• dbSNP Id: rs775288527
• ExAC: 17:2569395 CTT / C
• gnomAD v2: 17-2569395-CTT-C
• gnomAD v4: 17-2666101-CTT-C
• MyVariant Identifiers: chr17:g.2569396_2569397del (hg19) ; chr17:g.2666102_2666103del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2666106_2666107del , CM000679.2:g.2666106_2666107del	GRCh38
NC_000017.10:g.2569400_2569401del , CM000679.1:g.2569400_2569401del	GRCh37
NC_000017.9:g.2516150_2516151del	NCBI36
NG_009799.1:g.77478_77479del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.192+16_192+17del MANE Select	ENSP00000380378.4:n.192+16_192+17del
ENST00000674608.1:c.246+16_246+17del	ENSP00000501976.1:n.246+16_246+17del
ENST00000674717.1:c.-3-886_-3-885del	ENSP00000501931.1:n.-3-886_-3-885del
ENST00000675202.1:c.192+16_192+17del	ENSP00000502843.1:n.192+16_192+17del
ENST00000675331.1:c.192+16_192+17del	ENSP00000502031.1:n.192+16_192+17del
ENST00000675390.1:c.192+16_192+17del	ENSP00000501969.1:n.192+16_192+17del
ENST00000675430.1:n.419+16_419+17del
ENST00000675621.1:c.192+16_192+17del	ENSP00000502117.1:n.192+16_192+17del
ENST00000675764.1:c.*146+16_*146+17del	ENSP00000502242.1:n.*146+16_*146+17del
ENST00000676077.1:c.-4+16_-4+17del	ENSP00000502507.1:n.-4+16_-4+17del
ENST00000676098.1:c.192+16_192+17del	ENSP00000502735.1:n.192+16_192+17del
ENST00000676188.1:c.192+16_192+17del	ENSP00000502577.1:n.192+16_192+17del
ENST00000676201.1:n.346+16_346+17del
ENST00000676353.1:c.-4+16_-4+17del	ENSP00000502737.1:n.-4+16_-4+17del
ENST00000676456.1:n.297+16_297+17del
ENST00000397195.9:c.192+16_192+17del	ENSP00000380378.4:n.192+16_192+17del
ENST00000570400.1:c.*62+16_*62+17del	ENSP00000460258.1:n.*62+16_*62+17del
ENST00000572915.6:n.273-886_273-885del
ENST00000574816.5:n.31-10208_31-10207del
ENST00000576586.5:c.192+16_192+17del	ENSP00000461087.1:n.192+16_192+17del
ENST00000609078.1:n.151+16_151+17del
NM_000430.3:c.192+16_192+17del	NP_000421.1:n.192+16_192+17del
XM_011523901.1:c.246+16_246+17del	XP_011522203.1:n.246+16_246+17del
XM_011523902.1:c.246+16_246+17del	XP_011522204.1:n.246+16_246+17del
XM_011523903.1:c.246+16_246+17del	XP_011522205.1:n.246+16_246+17del
XM_011523904.1:c.246+16_246+17del	XP_011522206.1:n.246+16_246+17del
XM_011523901.2:c.246+16_246+17del	XP_011522203.1:n.246+16_246+17del
XM_011523902.3:c.246+16_246+17del	XP_011522204.1:n.246+16_246+17del
XM_011523903.2:c.246+16_246+17del	XP_011522205.1:n.246+16_246+17del
XM_017024701.1:c.192+16_192+17del	XP_016880190.1:n.192+16_192+17del
XM_017024702.2:c.-4+16_-4+17del	XP_016880191.1:n.-4+16_-4+17del
NM_000430.4:c.192+16_192+17del MANE Select	NP_000421.1:n.192+16_192+17del