Canonical Allele Identifier: CA397641948

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2577509A>T (hg19) ; chr17:g.2674215A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2674215A>T , CM000679.2:g.2674215A>T	GRCh38
NC_000017.10:g.2577509A>T , CM000679.1:g.2577509A>T	GRCh37
NC_000017.9:g.2524259A>T	NCBI36
NG_009799.1:g.85587A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.827A>T MANE Select	ENSP00000380378.4:p.Glu276Val
ENST00000571495.2:n.1912A>T
ENST00000674608.1:c.881A>T	ENSP00000501976.1:p.Glu294Val
ENST00000674717.1:c.632A>T	ENSP00000501931.1:p.Glu211Val
ENST00000675202.1:c.827A>T	ENSP00000502843.1:p.Glu276Val
ENST00000675331.1:c.827A>T	ENSP00000502031.1:p.Glu276Val
ENST00000675390.1:c.827A>T	ENSP00000501969.1:p.Glu276Val
ENST00000675574.1:n.1899A>T
ENST00000675621.1:c.827A>T	ENSP00000502117.1:p.Glu276Val
ENST00000675764.1:c.*781A>T	ENSP00000502242.1:n.*781A>T
ENST00000676077.1:c.*145A>T	ENSP00000502507.1:n.*145A>T
ENST00000676098.1:c.827A>T	ENSP00000502735.1:p.Glu276Val
ENST00000676188.1:c.827A>T	ENSP00000502577.1:p.Glu276Val
ENST00000676353.1:c.632A>T	ENSP00000502737.1:p.Glu211Val
ENST00000397193.7:n.635A>T
ENST00000397195.9:c.827A>T	ENSP00000380378.4:p.Glu276Val
ENST00000571495.1:n.551A>T
ENST00000572915.6:n.676+119A>T
ENST00000574468.1:c.323A>T	ENSP00000460591.1:p.Glu108Val
ENST00000574816.5:n.31-2099A>T
NM_000430.3:c.827A>T	NP_000421.1:p.Glu276Val
XM_011523901.1:c.881A>T	XP_011522203.1:p.Glu294Val
XM_011523902.1:c.881A>T	XP_011522204.1:p.Glu294Val
XM_011523903.1:c.881A>T	XP_011522205.1:p.Glu294Val
XM_011523901.2:c.881A>T	XP_011522203.1:p.Glu294Val
XM_011523902.3:c.881A>T	XP_011522204.1:p.Glu294Val
XM_011523903.2:c.881A>T	XP_011522205.1:p.Glu294Val
XM_017024701.1:c.827A>T	XP_016880190.1:p.Glu276Val
XM_017024702.2:c.632A>T	XP_016880191.1:p.Glu211Val
NM_000430.4:c.827A>T MANE Select	NP_000421.1:p.Glu276Val