Canonical Allele Identifier: CA2243479003

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2638292G= , CM000679.2:g.2638292G=	GRCh38
NC_000017.10:g.2541586G= , CM000679.1:g.2541586G=	GRCh37
NC_000017.9:g.2488336G=	NCBI36
NG_009799.1:g.49664G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.4G= MANE Select	ENSP00000380378.4:p.Val2=
ENST00000674608.1:c.4G=	ENSP00000501976.1:p.Val2=
ENST00000674717.1:c.-32G=	ENSP00000501931.1:n.-32G=
ENST00000675202.1:c.4G=	ENSP00000502843.1:p.Val2=
ENST00000675331.1:c.4G=	ENSP00000502031.1:p.Val2=
ENST00000675390.1:c.4G=	ENSP00000501969.1:p.Val2=
ENST00000675430.1:n.231G=
ENST00000675621.1:c.4G=	ENSP00000502117.1:p.Val2=
ENST00000675764.1:c.4G=	ENSP00000502242.1:p.Val2=
ENST00000676077.1:c.-163-27080G=	ENSP00000502507.1:n.-163-27080G=
ENST00000676098.1:c.4G=	ENSP00000502735.1:p.Val2=
ENST00000676188.1:c.4G=	ENSP00000502577.1:p.Val2=
ENST00000676201.1:n.243G=
ENST00000676353.1:c.-107G=	ENSP00000502737.1:n.-107G=
ENST00000676456.1:n.194G=
ENST00000397195.9:c.4G=	ENSP00000380378.4:p.Val2=
ENST00000570400.1:c.4G=	ENSP00000460258.1:p.Val2=
ENST00000571289.1:n.233G=
ENST00000572915.6:n.244G=
ENST00000574816.5:n.30+28724G=
ENST00000575477.5:n.591G=
ENST00000576586.5:c.4G=	ENSP00000461087.1:p.Val2=
NM_000430.3:c.4G=	NP_000421.1:p.Val2=
XM_011523901.1:c.4G=	XP_011522203.1:p.Val2=
XM_011523902.1:c.4G=	XP_011522204.1:p.Val2=
XM_011523903.1:c.4G=	XP_011522205.1:p.Val2=
XM_011523904.1:c.4G=	XP_011522206.1:p.Val2=
XM_011523901.2:c.4G=	XP_011522203.1:p.Val2=
XM_011523902.3:c.4G=	XP_011522204.1:p.Val2=
XM_011523903.2:c.4G=	XP_011522205.1:p.Val2=
XM_017024701.1:c.4G=	XP_016880190.1:p.Val2=
XM_017024702.2:c.-107G=	XP_016880191.1:n.-107G=
NM_000430.4:c.4G= MANE Select	NP_000421.1:p.Val2=