Canonical Allele Identifier: CA497474013

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2577405G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2674111G>C , CM000679.2:g.2674111G>C	GRCh38
NC_000017.10:g.2577405G>C , CM000679.1:g.2577405G>C	GRCh37
NC_000017.9:g.2524155G>C	NCBI36
NG_009799.1:g.85483G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.723G>C MANE Select	ENSP00000380378.4:p.Arg241=
ENST00000571495.2:n.1808G>C
ENST00000674608.1:c.777G>C	ENSP00000501976.1:p.Arg259=
ENST00000674717.1:c.528G>C	ENSP00000501931.1:p.Arg176=
ENST00000675202.1:c.723G>C	ENSP00000502843.1:p.Arg241=
ENST00000675331.1:c.723G>C	ENSP00000502031.1:p.Arg241=
ENST00000675390.1:c.723G>C	ENSP00000501969.1:p.Arg241=
ENST00000675574.1:n.1795G>C
ENST00000675621.1:c.723G>C	ENSP00000502117.1:p.Arg241=
ENST00000675764.1:c.*677G>C	ENSP00000502242.1:n.*677G>C
ENST00000676077.1:c.*41G>C	ENSP00000502507.1:n.*41G>C
ENST00000676098.1:c.723G>C	ENSP00000502735.1:p.Arg241=
ENST00000676188.1:c.723G>C	ENSP00000502577.1:p.Arg241=
ENST00000676353.1:c.528G>C	ENSP00000502737.1:p.Arg176=
ENST00000397193.7:n.531G>C
ENST00000397195.9:c.723G>C	ENSP00000380378.4:p.Arg241=
ENST00000571495.1:n.447G>C
ENST00000572915.6:n.676+15G>C
ENST00000574468.1:c.219G>C	ENSP00000460591.1:p.Arg73=
ENST00000574816.5:n.31-2203G>C
NM_000430.3:c.723G>C	NP_000421.1:p.Arg241=
XM_011523901.1:c.777G>C	XP_011522203.1:p.Arg259=
XM_011523902.1:c.777G>C	XP_011522204.1:p.Arg259=
XM_011523903.1:c.777G>C	XP_011522205.1:p.Arg259=
XM_011523904.1:c.*41G>C	XP_011522206.1:n.*41G>C
XM_011523901.2:c.777G>C	XP_011522203.1:p.Arg259=
XM_011523902.3:c.777G>C	XP_011522204.1:p.Arg259=
XM_011523903.2:c.777G>C	XP_011522205.1:p.Arg259=
XM_017024701.1:c.723G>C	XP_016880190.1:p.Arg241=
XM_017024702.2:c.528G>C	XP_016880191.1:p.Arg176=
NM_000430.4:c.723G>C MANE Select	NP_000421.1:p.Arg241=