Canonical Allele Identifier: CA919775588
Gene: PAFAH1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1011960547

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2665137_2665141del , CM000679.2:g.2665137_2665141del GRCh38
NC_000017.10:g.2568431_2568435del , CM000679.1:g.2568431_2568435del GRCh37
NC_000017.9:g.2515181_2515185del NCBI36
NG_009799.1:g.76509_76513del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.33-235_33-231del MANE Select ENSP00000380378.4:n.33-235_33-231del
ENST00000674608.1:c.87-235_87-231del ENSP00000501976.1:n.87-235_87-231del
ENST00000674717.1:c.-3-1855_-3-1851del ENSP00000501931.1:n.-3-1855_-3-1851del
ENST00000675202.1:c.33-235_33-231del ENSP00000502843.1:n.33-235_33-231del
ENST00000675331.1:c.33-235_33-231del ENSP00000502031.1:n.33-235_33-231del
ENST00000675390.1:c.33-235_33-231del ENSP00000501969.1:n.33-235_33-231del
ENST00000675430.1:n.260-235_260-231del
ENST00000675621.1:c.33-235_33-231del ENSP00000502117.1:n.33-235_33-231del
ENST00000675764.1:c.131-235_131-231del ENSP00000502242.1:n.131-235_131-231del
ENST00000676077.1:c.-163-235_-163-231del ENSP00000502507.1:n.-163-235_-163-231del
ENST00000676098.1:c.33-235_33-231del ENSP00000502735.1:n.33-235_33-231del
ENST00000676188.1:c.33-235_33-231del ENSP00000502577.1:n.33-235_33-231del
ENST00000676201.1:n.272-879_272-875del
ENST00000676353.1:c.-78-879_-78-875del ENSP00000502737.1:n.-78-879_-78-875del
ENST00000676456.1:n.223-879_223-875del
ENST00000397195.9:c.33-235_33-231del ENSP00000380378.4:n.33-235_33-231del
ENST00000570400.1:c.33-879_33-875del ENSP00000460258.1:n.33-879_33-875del
ENST00000572915.6:n.273-1855_273-1851del
ENST00000574816.5:n.31-11177_31-11173del
ENST00000575477.5:n.620-879_620-875del
ENST00000576586.5:c.33-235_33-231del ENSP00000461087.1:n.33-235_33-231del
NM_000430.3:c.33-235_33-231del NP_000421.1:n.33-235_33-231del
XM_011523901.1:c.87-235_87-231del XP_011522203.1:n.87-235_87-231del
XM_011523902.1:c.87-235_87-231del XP_011522204.1:n.87-235_87-231del
XM_011523903.1:c.87-235_87-231del XP_011522205.1:n.87-235_87-231del
XM_011523904.1:c.87-235_87-231del XP_011522206.1:n.87-235_87-231del
XM_011523901.2:c.87-235_87-231del XP_011522203.1:n.87-235_87-231del
XM_011523902.3:c.87-235_87-231del XP_011522204.1:n.87-235_87-231del
XM_011523903.2:c.87-235_87-231del XP_011522205.1:n.87-235_87-231del
XM_017024701.1:c.33-235_33-231del XP_016880190.1:n.33-235_33-231del
XM_017024702.2:c.-78-879_-78-875del XP_016880191.1:n.-78-879_-78-875del
NM_000430.4:c.33-235_33-231del MANE Select NP_000421.1:n.33-235_33-231del