Canonical Allele Identifier: CA2243490705

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2672730C= , CM000679.2:g.2672730C=	GRCh38
NC_000017.10:g.2576024C= , CM000679.1:g.2576024C=	GRCh37
NC_000017.9:g.2522774C=	NCBI36
NG_009799.1:g.84102C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.644C= MANE Select	ENSP00000380378.4:p.Thr215=
ENST00000571495.2:n.427C=
ENST00000674608.1:c.698C=	ENSP00000501976.1:p.Thr233=
ENST00000674717.1:c.449C=	ENSP00000501931.1:p.Thr150=
ENST00000675202.1:c.644C=	ENSP00000502843.1:p.Thr215=
ENST00000675331.1:c.644C=	ENSP00000502031.1:p.Thr215=
ENST00000675390.1:c.644C=	ENSP00000501969.1:p.Thr215=
ENST00000675574.1:n.414C=
ENST00000675621.1:c.644C=	ENSP00000502117.1:p.Thr215=
ENST00000675764.1:c.*598C=	ENSP00000502242.1:n.*598C=
ENST00000676077.1:c.374-1330C=	ENSP00000502507.1:n.374-1330C=
ENST00000676098.1:c.644C=	ENSP00000502735.1:p.Thr215=
ENST00000676188.1:c.644C=	ENSP00000502577.1:p.Thr215=
ENST00000676353.1:c.449C=	ENSP00000502737.1:p.Thr150=
ENST00000397193.7:n.452C=
ENST00000397195.9:c.644C=	ENSP00000380378.4:p.Thr215=
ENST00000572915.6:n.612C=
ENST00000574468.1:c.140C=	ENSP00000460591.1:p.Thr47=
ENST00000574816.5:n.31-3584C=
NM_000430.3:c.644C=	NP_000421.1:p.Thr215=
XM_011523901.1:c.698C=	XP_011522203.1:p.Thr233=
XM_011523902.1:c.698C=	XP_011522204.1:p.Thr233=
XM_011523903.1:c.698C=	XP_011522205.1:p.Thr233=
XM_011523904.1:c.623-1330C=	XP_011522206.1:n.623-1330C=
XM_011523901.2:c.698C=	XP_011522203.1:p.Thr233=
XM_011523902.3:c.698C=	XP_011522204.1:p.Thr233=
XM_011523903.2:c.698C=	XP_011522205.1:p.Thr233=
XM_017024701.1:c.644C=	XP_016880190.1:p.Thr215=
XM_017024702.2:c.449C=	XP_016880191.1:p.Thr150=
NM_000430.4:c.644C= MANE Select	NP_000421.1:p.Thr215=