Canonical Allele Identifier: CA497425679

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2579855T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676561T>C , CM000679.2:g.2676561T>C	GRCh38
NC_000017.10:g.2579855T>C , CM000679.1:g.2579855T>C	GRCh37
NC_000017.9:g.2526605T>C	NCBI36
NG_009799.1:g.87933T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397195.10:c.957T>C MANE Select	ENSP00000380378.4:p.Thr319=
ENST00000571495.2:n.2042T>C
ENST00000674608.1:c.1011T>C	ENSP00000501976.1:p.Thr337=
ENST00000674717.1:c.762T>C	ENSP00000501931.1:p.Thr254=
ENST00000675084.1:n.211T>C
ENST00000675202.1:c.957T>C	ENSP00000502843.1:p.Thr319=
ENST00000675331.1:c.957T>C	ENSP00000502031.1:p.Thr319=
ENST00000675385.1:n.571T>C
ENST00000675390.1:c.957T>C	ENSP00000501969.1:p.Thr319=
ENST00000675574.1:n.4012T>C
ENST00000675621.1:c.957T>C	ENSP00000502117.1:p.Thr319=
ENST00000675764.1:c.*911T>C	ENSP00000502242.1:n.*911T>C
ENST00000676077.1:c.*275T>C	ENSP00000502507.1:n.*275T>C
ENST00000676098.1:c.957T>C	ENSP00000502735.1:p.Thr319=
ENST00000676188.1:c.957T>C	ENSP00000502577.1:p.Thr319=
ENST00000676353.1:c.762T>C	ENSP00000502737.1:p.Thr254=
ENST00000397193.7:n.765T>C
ENST00000397195.9:c.957T>C	ENSP00000380378.4:p.Thr319=
ENST00000571495.1:n.681T>C
ENST00000572915.6:n.676+2465T>C
ENST00000574468.1:c.396+2273T>C	ENSP00000460591.1:n.396+2273T>C
ENST00000574816.5:n.278T>C
NM_000430.3:c.957T>C	NP_000421.1:p.Thr319=
XM_011523901.1:c.1011T>C	XP_011522203.1:p.Thr337=
XM_011523902.1:c.1011T>C	XP_011522204.1:p.Thr337=
XM_011523903.1:c.1011T>C	XP_011522205.1:p.Thr337=
XM_011523901.2:c.1011T>C	XP_011522203.1:p.Thr337=
XM_011523902.3:c.1011T>C	XP_011522204.1:p.Thr337=
XM_011523903.2:c.1011T>C	XP_011522205.1:p.Thr337=
XM_017024701.1:c.957T>C	XP_016880190.1:p.Thr319=
XM_017024702.2:c.762T>C	XP_016880191.1:p.Thr254=
NM_000430.4:c.957T>C MANE Select	NP_000421.1:p.Thr319=