Canonical Allele Identifier: CA497474020

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2577411T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2674117T>C , CM000679.2:g.2674117T>C	GRCh38
NC_000017.10:g.2577411T>C , CM000679.1:g.2577411T>C	GRCh37
NC_000017.9:g.2524161T>C	NCBI36
NG_009799.1:g.85489T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.729T>C MANE Select	ENSP00000380378.4:p.Asn243=
ENST00000571495.2:n.1814T>C
ENST00000674608.1:c.783T>C	ENSP00000501976.1:p.Asn261=
ENST00000674717.1:c.534T>C	ENSP00000501931.1:p.Asn178=
ENST00000675202.1:c.729T>C	ENSP00000502843.1:p.Asn243=
ENST00000675331.1:c.729T>C	ENSP00000502031.1:p.Asn243=
ENST00000675390.1:c.729T>C	ENSP00000501969.1:p.Asn243=
ENST00000675574.1:n.1801T>C
ENST00000675621.1:c.729T>C	ENSP00000502117.1:p.Asn243=
ENST00000675764.1:c.*683T>C	ENSP00000502242.1:n.*683T>C
ENST00000676077.1:c.*47T>C	ENSP00000502507.1:n.*47T>C
ENST00000676098.1:c.729T>C	ENSP00000502735.1:p.Asn243=
ENST00000676188.1:c.729T>C	ENSP00000502577.1:p.Asn243=
ENST00000676353.1:c.534T>C	ENSP00000502737.1:p.Asn178=
ENST00000397193.7:n.537T>C
ENST00000397195.9:c.729T>C	ENSP00000380378.4:p.Asn243=
ENST00000571495.1:n.453T>C
ENST00000572915.6:n.676+21T>C
ENST00000574468.1:c.225T>C	ENSP00000460591.1:p.Asn75=
ENST00000574816.5:n.31-2197T>C
NM_000430.3:c.729T>C	NP_000421.1:p.Asn243=
XM_011523901.1:c.783T>C	XP_011522203.1:p.Asn261=
XM_011523902.1:c.783T>C	XP_011522204.1:p.Asn261=
XM_011523903.1:c.783T>C	XP_011522205.1:p.Asn261=
XM_011523904.1:c.*47T>C	XP_011522206.1:n.*47T>C
XM_011523901.2:c.783T>C	XP_011522203.1:p.Asn261=
XM_011523902.3:c.783T>C	XP_011522204.1:p.Asn261=
XM_011523903.2:c.783T>C	XP_011522205.1:p.Asn261=
XM_017024701.1:c.729T>C	XP_016880190.1:p.Asn243=
XM_017024702.2:c.534T>C	XP_016880191.1:p.Asn178=
NM_000430.4:c.729T>C MANE Select	NP_000421.1:p.Asn243=