Canonical Allele Identifier: CA397642344

Gene: PAFAH1B1

Linked Data

• dbSNP Id: rs1452249667
• gnomAD v2: 17-2579896-C-T
• gnomAD v3: 17-2676602-C-T
• gnomAD v4: 17-2676602-C-T
• MyVariant Identifiers: chr17:g.2579896C>T (hg19) ; chr17:g.2676602C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676602C>T , CM000679.2:g.2676602C>T	GRCh38
NC_000017.10:g.2579896C>T , CM000679.1:g.2579896C>T	GRCh37
NC_000017.9:g.2526646C>T	NCBI36
NG_009799.1:g.87974C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.998C>T MANE Select	ENSP00000380378.4:p.Thr333Ile
ENST00000571495.2:n.2083C>T
ENST00000674608.1:c.1052C>T	ENSP00000501976.1:p.Thr351Ile
ENST00000674717.1:c.803C>T	ENSP00000501931.1:p.Thr268Ile
ENST00000675084.1:n.252C>T
ENST00000675202.1:c.998C>T	ENSP00000502843.1:p.Thr333Ile
ENST00000675331.1:c.998C>T	ENSP00000502031.1:p.Thr333Ile
ENST00000675385.1:n.612C>T
ENST00000675390.1:c.998C>T	ENSP00000501969.1:p.Thr333Ile
ENST00000675574.1:n.4053C>T
ENST00000675621.1:c.998C>T	ENSP00000502117.1:p.Thr333Ile
ENST00000675764.1:c.*952C>T	ENSP00000502242.1:n.*952C>T
ENST00000676077.1:c.*316C>T	ENSP00000502507.1:n.*316C>T
ENST00000676098.1:c.998C>T	ENSP00000502735.1:p.Thr333Ile
ENST00000676188.1:c.998C>T	ENSP00000502577.1:p.Thr333Ile
ENST00000676353.1:c.803C>T	ENSP00000502737.1:p.Thr268Ile
ENST00000397193.7:n.806C>T
ENST00000397195.9:c.998C>T	ENSP00000380378.4:p.Thr333Ile
ENST00000571495.1:n.722C>T
ENST00000572915.6:n.676+2506C>T
ENST00000574468.1:c.396+2314C>T	ENSP00000460591.1:n.396+2314C>T
ENST00000574816.5:n.319C>T
NM_000430.3:c.998C>T	NP_000421.1:p.Thr333Ile
XM_011523901.1:c.1052C>T	XP_011522203.1:p.Thr351Ile
XM_011523902.1:c.1052C>T	XP_011522204.1:p.Thr351Ile
XM_011523903.1:c.1052C>T	XP_011522205.1:p.Thr351Ile
XM_011523901.2:c.1052C>T	XP_011522203.1:p.Thr351Ile
XM_011523902.3:c.1052C>T	XP_011522204.1:p.Thr351Ile
XM_011523903.2:c.1052C>T	XP_011522205.1:p.Thr351Ile
XM_017024701.1:c.998C>T	XP_016880190.1:p.Thr333Ile
XM_017024702.2:c.803C>T	XP_016880191.1:p.Thr268Ile
NM_000430.4:c.998C>T MANE Select	NP_000421.1:p.Thr333Ile