Canonical Allele Identifier: CA2243491394

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2674112C= , CM000679.2:g.2674112C=	GRCh38
NC_000017.10:g.2577406C= , CM000679.1:g.2577406C=	GRCh37
NC_000017.9:g.2524156C=	NCBI36
NG_009799.1:g.85484C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.724C= MANE Select	ENSP00000380378.4:p.Pro242=
ENST00000571495.2:n.1809C=
ENST00000674608.1:c.778C=	ENSP00000501976.1:p.Pro260=
ENST00000674717.1:c.529C=	ENSP00000501931.1:p.Pro177=
ENST00000675202.1:c.724C=	ENSP00000502843.1:p.Pro242=
ENST00000675331.1:c.724C=	ENSP00000502031.1:p.Pro242=
ENST00000675390.1:c.724C=	ENSP00000501969.1:p.Pro242=
ENST00000675574.1:n.1796C=
ENST00000675621.1:c.724C=	ENSP00000502117.1:p.Pro242=
ENST00000675764.1:c.*678C=	ENSP00000502242.1:n.*678C=
ENST00000676077.1:c.*42C=	ENSP00000502507.1:n.*42C=
ENST00000676098.1:c.724C=	ENSP00000502735.1:p.Pro242=
ENST00000676188.1:c.724C=	ENSP00000502577.1:p.Pro242=
ENST00000676353.1:c.529C=	ENSP00000502737.1:p.Pro177=
ENST00000397193.7:n.532C=
ENST00000397195.9:c.724C=	ENSP00000380378.4:p.Pro242=
ENST00000571495.1:n.448C=
ENST00000572915.6:n.676+16C=
ENST00000574468.1:c.220C=	ENSP00000460591.1:p.Pro74=
ENST00000574816.5:n.31-2202C=
NM_000430.3:c.724C=	NP_000421.1:p.Pro242=
XM_011523901.1:c.778C=	XP_011522203.1:p.Pro260=
XM_011523902.1:c.778C=	XP_011522204.1:p.Pro260=
XM_011523903.1:c.778C=	XP_011522205.1:p.Pro260=
XM_011523904.1:c.*42C=	XP_011522206.1:n.*42C=
XM_011523901.2:c.778C=	XP_011522203.1:p.Pro260=
XM_011523902.3:c.778C=	XP_011522204.1:p.Pro260=
XM_011523903.2:c.778C=	XP_011522205.1:p.Pro260=
XM_017024701.1:c.724C=	XP_016880190.1:p.Pro242=
XM_017024702.2:c.529C=	XP_016880191.1:p.Pro177=
NM_000430.4:c.724C= MANE Select	NP_000421.1:p.Pro242=