Canonical Allele Identifier: CA397642339

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2579895A>C (hg19) ; chr17:g.2676601A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676601A>C , CM000679.2:g.2676601A>C	GRCh38
NC_000017.10:g.2579895A>C , CM000679.1:g.2579895A>C	GRCh37
NC_000017.9:g.2526645A>C	NCBI36
NG_009799.1:g.87973A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.997A>C MANE Select	ENSP00000380378.4:p.Thr333Pro
ENST00000571495.2:n.2082A>C
ENST00000674608.1:c.1051A>C	ENSP00000501976.1:p.Thr351Pro
ENST00000674717.1:c.802A>C	ENSP00000501931.1:p.Thr268Pro
ENST00000675084.1:n.251A>C
ENST00000675202.1:c.997A>C	ENSP00000502843.1:p.Thr333Pro
ENST00000675331.1:c.997A>C	ENSP00000502031.1:p.Thr333Pro
ENST00000675385.1:n.611A>C
ENST00000675390.1:c.997A>C	ENSP00000501969.1:p.Thr333Pro
ENST00000675574.1:n.4052A>C
ENST00000675621.1:c.997A>C	ENSP00000502117.1:p.Thr333Pro
ENST00000675764.1:c.*951A>C	ENSP00000502242.1:n.*951A>C
ENST00000676077.1:c.*315A>C	ENSP00000502507.1:n.*315A>C
ENST00000676098.1:c.997A>C	ENSP00000502735.1:p.Thr333Pro
ENST00000676188.1:c.997A>C	ENSP00000502577.1:p.Thr333Pro
ENST00000676353.1:c.802A>C	ENSP00000502737.1:p.Thr268Pro
ENST00000397193.7:n.805A>C
ENST00000397195.9:c.997A>C	ENSP00000380378.4:p.Thr333Pro
ENST00000571495.1:n.721A>C
ENST00000572915.6:n.676+2505A>C
ENST00000574468.1:c.396+2313A>C	ENSP00000460591.1:n.396+2313A>C
ENST00000574816.5:n.318A>C
NM_000430.3:c.997A>C	NP_000421.1:p.Thr333Pro
XM_011523901.1:c.1051A>C	XP_011522203.1:p.Thr351Pro
XM_011523902.1:c.1051A>C	XP_011522204.1:p.Thr351Pro
XM_011523903.1:c.1051A>C	XP_011522205.1:p.Thr351Pro
XM_011523901.2:c.1051A>C	XP_011522203.1:p.Thr351Pro
XM_011523902.3:c.1051A>C	XP_011522204.1:p.Thr351Pro
XM_011523903.2:c.1051A>C	XP_011522205.1:p.Thr351Pro
XM_017024701.1:c.997A>C	XP_016880190.1:p.Thr333Pro
XM_017024702.2:c.802A>C	XP_016880191.1:p.Thr268Pro
NM_000430.4:c.997A>C MANE Select	NP_000421.1:p.Thr333Pro