Canonical Allele Identifier: CA2243492516

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676584C= , CM000679.2:g.2676584C=	GRCh38
NC_000017.10:g.2579878C= , CM000679.1:g.2579878C=	GRCh37
NC_000017.9:g.2526628C=	NCBI36
NG_009799.1:g.87956C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.980C= MANE Select	ENSP00000380378.4:p.Thr327=
ENST00000571495.2:n.2065C=
ENST00000674608.1:c.1034C=	ENSP00000501976.1:p.Thr345=
ENST00000674717.1:c.785C=	ENSP00000501931.1:p.Thr262=
ENST00000675084.1:n.234C=
ENST00000675202.1:c.980C=	ENSP00000502843.1:p.Thr327=
ENST00000675331.1:c.980C=	ENSP00000502031.1:p.Thr327=
ENST00000675385.1:n.594C=
ENST00000675390.1:c.980C=	ENSP00000501969.1:p.Thr327=
ENST00000675574.1:n.4035C=
ENST00000675621.1:c.980C=	ENSP00000502117.1:p.Thr327=
ENST00000675764.1:c.*934C=	ENSP00000502242.1:n.*934C=
ENST00000676077.1:c.*298C=	ENSP00000502507.1:n.*298C=
ENST00000676098.1:c.980C=	ENSP00000502735.1:p.Thr327=
ENST00000676188.1:c.980C=	ENSP00000502577.1:p.Thr327=
ENST00000676353.1:c.785C=	ENSP00000502737.1:p.Thr262=
ENST00000397193.7:n.788C=
ENST00000397195.9:c.980C=	ENSP00000380378.4:p.Thr327=
ENST00000571495.1:n.704C=
ENST00000572915.6:n.676+2488C=
ENST00000574468.1:c.396+2296C=	ENSP00000460591.1:n.396+2296C=
ENST00000574816.5:n.301C=
NM_000430.3:c.980C=	NP_000421.1:p.Thr327=
XM_011523901.1:c.1034C=	XP_011522203.1:p.Thr345=
XM_011523902.1:c.1034C=	XP_011522204.1:p.Thr345=
XM_011523903.1:c.1034C=	XP_011522205.1:p.Thr345=
XM_011523901.2:c.1034C=	XP_011522203.1:p.Thr345=
XM_011523902.3:c.1034C=	XP_011522204.1:p.Thr345=
XM_011523903.2:c.1034C=	XP_011522205.1:p.Thr345=
XM_017024701.1:c.980C=	XP_016880190.1:p.Thr327=
XM_017024702.2:c.785C=	XP_016880191.1:p.Thr262=
NM_000430.4:c.980C= MANE Select	NP_000421.1:p.Thr327=