Canonical Allele Identifier: CA272447

Gene: PAFAH1B1

Linked Data

• ClinVar Variation Id: 159547
• ClinVar RCV Id: RCV000147064
• dbSNP Id: rs369259961
• MyVariant Identifiers: chr17:g.2568717T>G (hg19) ; chr17:g.2665423T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2665423T>G , CM000679.2:g.2665423T>G	GRCh38
NC_000017.10:g.2568717T>G , CM000679.1:g.2568717T>G	GRCh37
NC_000017.9:g.2515467T>G	NCBI36
NG_009799.1:g.76795T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.84T>G MANE Select	ENSP00000380378.4:p.Tyr28Ter
ENST00000674608.1:c.138T>G	ENSP00000501976.1:p.Tyr46Ter
ENST00000674717.1:c.-3-1569T>G	ENSP00000501931.1:n.-3-1569T>G
ENST00000675202.1:c.84T>G	ENSP00000502843.1:p.Tyr28Ter
ENST00000675331.1:c.84T>G	ENSP00000502031.1:p.Tyr28Ter
ENST00000675390.1:c.84T>G	ENSP00000501969.1:p.Tyr28Ter
ENST00000675430.1:n.311T>G
ENST00000675621.1:c.84T>G	ENSP00000502117.1:p.Tyr28Ter
ENST00000675764.1:c.*38T>G	ENSP00000502242.1:n.*38T>G
ENST00000676077.1:c.-112T>G	ENSP00000502507.1:n.-112T>G
ENST00000676098.1:c.84T>G	ENSP00000502735.1:p.Tyr28Ter
ENST00000676188.1:c.84T>G	ENSP00000502577.1:p.Tyr28Ter
ENST00000676201.1:n.272-593T>G
ENST00000676353.1:c.-78-593T>G	ENSP00000502737.1:n.-78-593T>G
ENST00000676456.1:n.223-593T>G
ENST00000397195.9:c.84T>G	ENSP00000380378.4:p.Tyr28Ter
ENST00000570400.1:c.33-593T>G	ENSP00000460258.1:n.33-593T>G
ENST00000572915.6:n.273-1569T>G
ENST00000574816.5:n.31-10891T>G
ENST00000575477.5:n.620-593T>G
ENST00000576586.5:c.84T>G	ENSP00000461087.1:p.Tyr28Ter
ENST00000609078.1:n.43T>G
NM_000430.3:c.84T>G	NP_000421.1:p.Tyr28Ter
XM_011523901.1:c.138T>G	XP_011522203.1:p.Tyr46Ter
XM_011523902.1:c.138T>G	XP_011522204.1:p.Tyr46Ter
XM_011523903.1:c.138T>G	XP_011522205.1:p.Tyr46Ter
XM_011523904.1:c.138T>G	XP_011522206.1:p.Tyr46Ter
XM_011523901.2:c.138T>G	XP_011522203.1:p.Tyr46Ter
XM_011523902.3:c.138T>G	XP_011522204.1:p.Tyr46Ter
XM_011523903.2:c.138T>G	XP_011522205.1:p.Tyr46Ter
XM_017024701.1:c.84T>G	XP_016880190.1:p.Tyr28Ter
XM_017024702.2:c.-78-593T>G	XP_016880191.1:n.-78-593T>G
NM_000430.4:c.84T>G MANE Select	NP_000421.1:p.Tyr28Ter