Canonical Allele Identifier: CA2243487577
Gene: PAFAH1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2666018T= , CM000679.2:g.2666018T= GRCh38
NC_000017.10:g.2569312T= , CM000679.1:g.2569312T= GRCh37
NC_000017.9:g.2516062T= NCBI36
NG_009799.1:g.77390T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.120T= MANE Select ENSP00000380378.4:p.Asn40=
ENST00000674608.1:c.174T= ENSP00000501976.1:p.Asn58=
ENST00000674717.1:c.-3-974T= ENSP00000501931.1:n.-3-974T=
ENST00000675202.1:c.120T= ENSP00000502843.1:p.Asn40=
ENST00000675331.1:c.120T= ENSP00000502031.1:p.Asn40=
ENST00000675390.1:c.120T= ENSP00000501969.1:p.Asn40=
ENST00000675430.1:n.347T=
ENST00000675621.1:c.120T= ENSP00000502117.1:p.Asn40=
ENST00000675764.1:c.*74T= ENSP00000502242.1:n.*74T=
ENST00000676077.1:c.-76T= ENSP00000502507.1:n.-76T=
ENST00000676098.1:c.120T= ENSP00000502735.1:p.Asn40=
ENST00000676188.1:c.120T= ENSP00000502577.1:p.Asn40=
ENST00000676201.1:n.274T=
ENST00000676353.1:c.-76T= ENSP00000502737.1:n.-76T=
ENST00000676456.1:n.225T=
ENST00000397195.9:c.120T= ENSP00000380378.4:p.Asn40=
ENST00000570400.1:c.35T= ENSP00000460258.1:p.Met12=
ENST00000572915.6:n.273-974T=
ENST00000574816.5:n.31-10296T=
ENST00000575477.5:n.622T=
ENST00000576586.5:c.120T= ENSP00000461087.1:p.Asn40=
ENST00000609078.1:n.79T=
NM_000430.3:c.120T= NP_000421.1:p.Asn40=
XM_011523901.1:c.174T= XP_011522203.1:p.Asn58=
XM_011523902.1:c.174T= XP_011522204.1:p.Asn58=
XM_011523903.1:c.174T= XP_011522205.1:p.Asn58=
XM_011523904.1:c.174T= XP_011522206.1:p.Asn58=
XM_011523901.2:c.174T= XP_011522203.1:p.Asn58=
XM_011523902.3:c.174T= XP_011522204.1:p.Asn58=
XM_011523903.2:c.174T= XP_011522205.1:p.Asn58=
XM_017024701.1:c.120T= XP_016880190.1:p.Asn40=
XM_017024702.2:c.-76T= XP_016880191.1:n.-76T=
NM_000430.4:c.120T= MANE Select NP_000421.1:p.Asn40=