Canonical Allele Identifier: CA397642292

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2579875G>C (hg19) ; chr17:g.2676581G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676581G>C , CM000679.2:g.2676581G>C	GRCh38
NC_000017.10:g.2579875G>C , CM000679.1:g.2579875G>C	GRCh37
NC_000017.9:g.2526625G>C	NCBI36
NG_009799.1:g.87953G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.977G>C MANE Select	ENSP00000380378.4:p.Ser326Thr
ENST00000571495.2:n.2062G>C
ENST00000674608.1:c.1031G>C	ENSP00000501976.1:p.Ser344Thr
ENST00000674717.1:c.782G>C	ENSP00000501931.1:p.Ser261Thr
ENST00000675084.1:n.231G>C
ENST00000675202.1:c.977G>C	ENSP00000502843.1:p.Ser326Thr
ENST00000675331.1:c.977G>C	ENSP00000502031.1:p.Ser326Thr
ENST00000675385.1:n.591G>C
ENST00000675390.1:c.977G>C	ENSP00000501969.1:p.Ser326Thr
ENST00000675574.1:n.4032G>C
ENST00000675621.1:c.977G>C	ENSP00000502117.1:p.Ser326Thr
ENST00000675764.1:c.*931G>C	ENSP00000502242.1:n.*931G>C
ENST00000676077.1:c.*295G>C	ENSP00000502507.1:n.*295G>C
ENST00000676098.1:c.977G>C	ENSP00000502735.1:p.Ser326Thr
ENST00000676188.1:c.977G>C	ENSP00000502577.1:p.Ser326Thr
ENST00000676353.1:c.782G>C	ENSP00000502737.1:p.Ser261Thr
ENST00000397193.7:n.785G>C
ENST00000397195.9:c.977G>C	ENSP00000380378.4:p.Ser326Thr
ENST00000571495.1:n.701G>C
ENST00000572915.6:n.676+2485G>C
ENST00000574468.1:c.396+2293G>C	ENSP00000460591.1:n.396+2293G>C
ENST00000574816.5:n.298G>C
NM_000430.3:c.977G>C	NP_000421.1:p.Ser326Thr
XM_011523901.1:c.1031G>C	XP_011522203.1:p.Ser344Thr
XM_011523902.1:c.1031G>C	XP_011522204.1:p.Ser344Thr
XM_011523903.1:c.1031G>C	XP_011522205.1:p.Ser344Thr
XM_011523901.2:c.1031G>C	XP_011522203.1:p.Ser344Thr
XM_011523902.3:c.1031G>C	XP_011522204.1:p.Ser344Thr
XM_011523903.2:c.1031G>C	XP_011522205.1:p.Ser344Thr
XM_017024701.1:c.977G>C	XP_016880190.1:p.Ser326Thr
XM_017024702.2:c.782G>C	XP_016880191.1:p.Ser261Thr
NM_000430.4:c.977G>C MANE Select	NP_000421.1:p.Ser326Thr