Canonical Allele Identifier: CA397641479

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2576035T>A (hg19) ; chr17:g.2672741T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2672741T>A , CM000679.2:g.2672741T>A	GRCh38
NC_000017.10:g.2576035T>A , CM000679.1:g.2576035T>A	GRCh37
NC_000017.9:g.2522785T>A	NCBI36
NG_009799.1:g.84113T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.655T>A MANE Select	ENSP00000380378.4:p.Trp219Arg
ENST00000571495.2:n.438T>A
ENST00000674608.1:c.709T>A	ENSP00000501976.1:p.Trp237Arg
ENST00000674717.1:c.460T>A	ENSP00000501931.1:p.Trp154Arg
ENST00000675202.1:c.655T>A	ENSP00000502843.1:p.Trp219Arg
ENST00000675331.1:c.655T>A	ENSP00000502031.1:p.Trp219Arg
ENST00000675390.1:c.655T>A	ENSP00000501969.1:p.Trp219Arg
ENST00000675574.1:n.425T>A
ENST00000675621.1:c.655T>A	ENSP00000502117.1:p.Trp219Arg
ENST00000675764.1:c.*609T>A	ENSP00000502242.1:n.*609T>A
ENST00000676077.1:c.374-1319T>A	ENSP00000502507.1:n.374-1319T>A
ENST00000676098.1:c.655T>A	ENSP00000502735.1:p.Trp219Arg
ENST00000676188.1:c.655T>A	ENSP00000502577.1:p.Trp219Arg
ENST00000676353.1:c.460T>A	ENSP00000502737.1:p.Trp154Arg
ENST00000397193.7:n.463T>A
ENST00000397195.9:c.655T>A	ENSP00000380378.4:p.Trp219Arg
ENST00000572915.6:n.623T>A
ENST00000574468.1:c.151T>A	ENSP00000460591.1:p.Trp51Arg
ENST00000574816.5:n.31-3573T>A
NM_000430.3:c.655T>A	NP_000421.1:p.Trp219Arg
XM_011523901.1:c.709T>A	XP_011522203.1:p.Trp237Arg
XM_011523902.1:c.709T>A	XP_011522204.1:p.Trp237Arg
XM_011523903.1:c.709T>A	XP_011522205.1:p.Trp237Arg
XM_011523904.1:c.623-1319T>A	XP_011522206.1:n.623-1319T>A
XM_011523901.2:c.709T>A	XP_011522203.1:p.Trp237Arg
XM_011523902.3:c.709T>A	XP_011522204.1:p.Trp237Arg
XM_011523903.2:c.709T>A	XP_011522205.1:p.Trp237Arg
XM_017024701.1:c.655T>A	XP_016880190.1:p.Trp219Arg
XM_017024702.2:c.460T>A	XP_016880191.1:p.Trp154Arg
NM_000430.4:c.655T>A MANE Select	NP_000421.1:p.Trp219Arg