Canonical Allele Identifier: CA497473730

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2577570A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2674276A>C , CM000679.2:g.2674276A>C	GRCh38
NC_000017.10:g.2577570A>C , CM000679.1:g.2577570A>C	GRCh37
NC_000017.9:g.2524320A>C	NCBI36
NG_009799.1:g.85648A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.888A>C MANE Select	ENSP00000380378.4:p.Ala296=
ENST00000571495.2:n.1973A>C
ENST00000674608.1:c.942A>C	ENSP00000501976.1:p.Ala314=
ENST00000674717.1:c.693A>C	ENSP00000501931.1:p.Ala231=
ENST00000675202.1:c.888A>C	ENSP00000502843.1:p.Ala296=
ENST00000675331.1:c.888A>C	ENSP00000502031.1:p.Ala296=
ENST00000675390.1:c.888A>C	ENSP00000501969.1:p.Ala296=
ENST00000675574.1:n.1960A>C
ENST00000675621.1:c.888A>C	ENSP00000502117.1:p.Ala296=
ENST00000675764.1:c.*842A>C	ENSP00000502242.1:n.*842A>C
ENST00000676077.1:c.*206A>C	ENSP00000502507.1:n.*206A>C
ENST00000676098.1:c.888A>C	ENSP00000502735.1:p.Ala296=
ENST00000676188.1:c.888A>C	ENSP00000502577.1:p.Ala296=
ENST00000676353.1:c.693A>C	ENSP00000502737.1:p.Ala231=
ENST00000397193.7:n.696A>C
ENST00000397195.9:c.888A>C	ENSP00000380378.4:p.Ala296=
ENST00000571495.1:n.612A>C
ENST00000572915.6:n.676+180A>C
ENST00000574468.1:c.384A>C	ENSP00000460591.1:p.Ala128=
ENST00000574816.5:n.31-2038A>C
NM_000430.3:c.888A>C	NP_000421.1:p.Ala296=
XM_011523901.1:c.942A>C	XP_011522203.1:p.Ala314=
XM_011523902.1:c.942A>C	XP_011522204.1:p.Ala314=
XM_011523903.1:c.942A>C	XP_011522205.1:p.Ala314=
XM_011523901.2:c.942A>C	XP_011522203.1:p.Ala314=
XM_011523902.3:c.942A>C	XP_011522204.1:p.Ala314=
XM_011523903.2:c.942A>C	XP_011522205.1:p.Ala314=
XM_017024701.1:c.888A>C	XP_016880190.1:p.Ala296=
XM_017024702.2:c.693A>C	XP_016880191.1:p.Ala231=
NM_000430.4:c.888A>C MANE Select	NP_000421.1:p.Ala296=