Canonical Allele Identifier: CA2243490700

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2672709T= , CM000679.2:g.2672709T=	GRCh38
NC_000017.10:g.2576003T= , CM000679.1:g.2576003T=	GRCh37
NC_000017.9:g.2522753T=	NCBI36
NG_009799.1:g.84081T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.623T= MANE Select	ENSP00000380378.4:p.Val208=
ENST00000571495.2:n.406T=
ENST00000674608.1:c.677T=	ENSP00000501976.1:p.Val226=
ENST00000674717.1:c.428T=	ENSP00000501931.1:p.Val143=
ENST00000675202.1:c.623T=	ENSP00000502843.1:p.Val208=
ENST00000675331.1:c.623T=	ENSP00000502031.1:p.Val208=
ENST00000675390.1:c.623T=	ENSP00000501969.1:p.Val208=
ENST00000675574.1:n.393T=
ENST00000675621.1:c.623T=	ENSP00000502117.1:p.Val208=
ENST00000675764.1:c.*577T=	ENSP00000502242.1:n.*577T=
ENST00000676077.1:c.374-1351T=	ENSP00000502507.1:n.374-1351T=
ENST00000676098.1:c.623T=	ENSP00000502735.1:p.Val208=
ENST00000676188.1:c.623T=	ENSP00000502577.1:p.Val208=
ENST00000676353.1:c.428T=	ENSP00000502737.1:p.Val143=
ENST00000397193.7:n.431T=
ENST00000397195.9:c.623T=	ENSP00000380378.4:p.Val208=
ENST00000572915.6:n.591T=
ENST00000574468.1:c.119T=	ENSP00000460591.1:p.Val40=
ENST00000574816.5:n.31-3605T=
NM_000430.3:c.623T=	NP_000421.1:p.Val208=
XM_011523901.1:c.677T=	XP_011522203.1:p.Val226=
XM_011523902.1:c.677T=	XP_011522204.1:p.Val226=
XM_011523903.1:c.677T=	XP_011522205.1:p.Val226=
XM_011523904.1:c.623-1351T=	XP_011522206.1:n.623-1351T=
XM_011523901.2:c.677T=	XP_011522203.1:p.Val226=
XM_011523902.3:c.677T=	XP_011522204.1:p.Val226=
XM_011523903.2:c.677T=	XP_011522205.1:p.Val226=
XM_017024701.1:c.623T=	XP_016880190.1:p.Val208=
XM_017024702.2:c.428T=	XP_016880191.1:p.Val143=
NM_000430.4:c.623T= MANE Select	NP_000421.1:p.Val208=