Canonical Allele Identifier: CA2243489477
Gene: PAFAH1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2670185A= , CM000679.2:g.2670185A= GRCh38
NC_000017.10:g.2573479A= , CM000679.1:g.2573479A= GRCh37
NC_000017.9:g.2520229A= NCBI36
NG_009799.1:g.81557A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.422A= MANE Select ENSP00000380378.4:p.Asp141=
ENST00000674608.1:c.476A= ENSP00000501976.1:p.Asp159=
ENST00000674717.1:c.227A= ENSP00000501931.1:p.Asp76=
ENST00000675202.1:c.422A= ENSP00000502843.1:p.Asp141=
ENST00000675331.1:c.422A= ENSP00000502031.1:p.Asp141=
ENST00000675390.1:c.422A= ENSP00000501969.1:p.Asp141=
ENST00000675430.1:n.649A=
ENST00000675621.1:c.422A= ENSP00000502117.1:p.Asp141=
ENST00000675764.1:c.*376A= ENSP00000502242.1:n.*376A=
ENST00000676077.1:c.227A= ENSP00000502507.1:p.Asp76=
ENST00000676098.1:c.422A= ENSP00000502735.1:p.Asp141=
ENST00000676188.1:c.422A= ENSP00000502577.1:p.Asp141=
ENST00000676201.1:n.576A=
ENST00000676353.1:c.227A= ENSP00000502737.1:p.Asp76=
ENST00000676456.1:n.527A=
ENST00000397193.7:n.230A=
ENST00000397195.9:c.422A= ENSP00000380378.4:p.Asp141=
ENST00000572915.6:n.480-90A=
ENST00000574816.5:n.31-6129A=
ENST00000609078.1:n.381A=
NM_000430.3:c.422A= NP_000421.1:p.Asp141=
XM_011523901.1:c.476A= XP_011522203.1:p.Asp159=
XM_011523902.1:c.476A= XP_011522204.1:p.Asp159=
XM_011523903.1:c.476A= XP_011522205.1:p.Asp159=
XM_011523904.1:c.476A= XP_011522206.1:p.Asp159=
XM_011523901.2:c.476A= XP_011522203.1:p.Asp159=
XM_011523902.3:c.476A= XP_011522204.1:p.Asp159=
XM_011523903.2:c.476A= XP_011522205.1:p.Asp159=
XM_017024701.1:c.422A= XP_016880190.1:p.Asp141=
XM_017024702.2:c.227A= XP_016880191.1:p.Asp76=
NM_000430.4:c.422A= MANE Select NP_000421.1:p.Asp141=