Canonical Allele Identifier: CA397638824
Gene: PAFAH1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2667097G>A , CM000679.2:g.2667097G>A GRCh38
NC_000017.10:g.2570391G>A , CM000679.1:g.2570391G>A GRCh37
NC_000017.9:g.2517141G>A NCBI36
NG_009799.1:g.78469G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000397195.10:c.298G>A MANE Select ENSP00000380378.4:p.Glu100Lys
ENST00000674608.1:c.352G>A ENSP00000501976.1:p.Glu118Lys
ENST00000674717.1:c.103G>A ENSP00000501931.1:p.Glu35Lys
ENST00000675202.1:c.298G>A ENSP00000502843.1:p.Glu100Lys
ENST00000675331.1:c.298G>A ENSP00000502031.1:p.Glu100Lys
ENST00000675390.1:c.298G>A ENSP00000501969.1:p.Glu100Lys
ENST00000675430.1:n.525G>A
ENST00000675621.1:c.298G>A ENSP00000502117.1:p.Glu100Lys
ENST00000675764.1:c.*252G>A ENSP00000502242.1:n.*252G>A
ENST00000676077.1:c.103G>A ENSP00000502507.1:p.Glu35Lys
ENST00000676098.1:c.298G>A ENSP00000502735.1:p.Glu100Lys
ENST00000676188.1:c.298G>A ENSP00000502577.1:p.Glu100Lys
ENST00000676201.1:n.452G>A
ENST00000676353.1:c.103G>A ENSP00000502737.1:p.Glu35Lys
ENST00000676456.1:n.403G>A
ENST00000397195.9:c.298G>A ENSP00000380378.4:p.Glu100Lys
ENST00000570400.1:c.*168G>A ENSP00000460258.1:n.*168G>A
ENST00000572915.6:n.378G>A
ENST00000574816.5:n.31-9217G>A
ENST00000609078.1:n.257G>A
NM_000430.3:c.298G>A NP_000421.1:p.Glu100Lys
XM_011523901.1:c.352G>A XP_011522203.1:p.Glu118Lys
XM_011523902.1:c.352G>A XP_011522204.1:p.Glu118Lys
XM_011523903.1:c.352G>A XP_011522205.1:p.Glu118Lys
XM_011523904.1:c.352G>A XP_011522206.1:p.Glu118Lys
XM_011523901.2:c.352G>A XP_011522203.1:p.Glu118Lys
XM_011523902.3:c.352G>A XP_011522204.1:p.Glu118Lys
XM_011523903.2:c.352G>A XP_011522205.1:p.Glu118Lys
XM_017024701.1:c.298G>A XP_016880190.1:p.Glu100Lys
XM_017024702.2:c.103G>A XP_016880191.1:p.Glu35Lys
NM_000430.4:c.298G>A MANE Select NP_000421.1:p.Glu100Lys