Canonical Allele Identifier: CA397642237

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2579853A>C (hg19) ; chr17:g.2676559A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676559A>C , CM000679.2:g.2676559A>C	GRCh38
NC_000017.10:g.2579853A>C , CM000679.1:g.2579853A>C	GRCh37
NC_000017.9:g.2526603A>C	NCBI36
NG_009799.1:g.87931A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.955A>C MANE Select	ENSP00000380378.4:p.Thr319Pro
ENST00000571495.2:n.2040A>C
ENST00000674608.1:c.1009A>C	ENSP00000501976.1:p.Thr337Pro
ENST00000674717.1:c.760A>C	ENSP00000501931.1:p.Thr254Pro
ENST00000675084.1:n.209A>C
ENST00000675202.1:c.955A>C	ENSP00000502843.1:p.Thr319Pro
ENST00000675331.1:c.955A>C	ENSP00000502031.1:p.Thr319Pro
ENST00000675385.1:n.569A>C
ENST00000675390.1:c.955A>C	ENSP00000501969.1:p.Thr319Pro
ENST00000675574.1:n.4010A>C
ENST00000675621.1:c.955A>C	ENSP00000502117.1:p.Thr319Pro
ENST00000675764.1:c.*909A>C	ENSP00000502242.1:n.*909A>C
ENST00000676077.1:c.*273A>C	ENSP00000502507.1:n.*273A>C
ENST00000676098.1:c.955A>C	ENSP00000502735.1:p.Thr319Pro
ENST00000676188.1:c.955A>C	ENSP00000502577.1:p.Thr319Pro
ENST00000676353.1:c.760A>C	ENSP00000502737.1:p.Thr254Pro
ENST00000397193.7:n.763A>C
ENST00000397195.9:c.955A>C	ENSP00000380378.4:p.Thr319Pro
ENST00000571495.1:n.679A>C
ENST00000572915.6:n.676+2463A>C
ENST00000574468.1:c.396+2271A>C	ENSP00000460591.1:n.396+2271A>C
ENST00000574816.5:n.276A>C
NM_000430.3:c.955A>C	NP_000421.1:p.Thr319Pro
XM_011523901.1:c.1009A>C	XP_011522203.1:p.Thr337Pro
XM_011523902.1:c.1009A>C	XP_011522204.1:p.Thr337Pro
XM_011523903.1:c.1009A>C	XP_011522205.1:p.Thr337Pro
XM_011523901.2:c.1009A>C	XP_011522203.1:p.Thr337Pro
XM_011523902.3:c.1009A>C	XP_011522204.1:p.Thr337Pro
XM_011523903.2:c.1009A>C	XP_011522205.1:p.Thr337Pro
XM_017024701.1:c.955A>C	XP_016880190.1:p.Thr319Pro
XM_017024702.2:c.760A>C	XP_016880191.1:p.Thr254Pro
NM_000430.4:c.955A>C MANE Select	NP_000421.1:p.Thr319Pro