Canonical Allele Identifier: CA397642177

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2579824C>G (hg19) ; chr17:g.2676530C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676530C>G , CM000679.2:g.2676530C>G	GRCh38
NC_000017.10:g.2579824C>G , CM000679.1:g.2579824C>G	GRCh37
NC_000017.9:g.2526574C>G	NCBI36
NG_009799.1:g.87902C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.926C>G MANE Select	ENSP00000380378.4:p.Pro309Arg
ENST00000571495.2:n.2011C>G
ENST00000674608.1:c.980C>G	ENSP00000501976.1:p.Pro327Arg
ENST00000674717.1:c.731C>G	ENSP00000501931.1:p.Pro244Arg
ENST00000675084.1:n.180C>G
ENST00000675202.1:c.926C>G	ENSP00000502843.1:p.Pro309Arg
ENST00000675331.1:c.926C>G	ENSP00000502031.1:p.Pro309Arg
ENST00000675385.1:n.540C>G
ENST00000675390.1:c.926C>G	ENSP00000501969.1:p.Pro309Arg
ENST00000675574.1:n.3981C>G
ENST00000675621.1:c.926C>G	ENSP00000502117.1:p.Pro309Arg
ENST00000675764.1:c.*880C>G	ENSP00000502242.1:n.*880C>G
ENST00000676077.1:c.*244C>G	ENSP00000502507.1:n.*244C>G
ENST00000676098.1:c.926C>G	ENSP00000502735.1:p.Pro309Arg
ENST00000676188.1:c.926C>G	ENSP00000502577.1:p.Pro309Arg
ENST00000676353.1:c.731C>G	ENSP00000502737.1:p.Pro244Arg
ENST00000397193.7:n.734C>G
ENST00000397195.9:c.926C>G	ENSP00000380378.4:p.Pro309Arg
ENST00000571495.1:n.650C>G
ENST00000572915.6:n.676+2434C>G
ENST00000574468.1:c.396+2242C>G	ENSP00000460591.1:n.396+2242C>G
ENST00000574816.5:n.247C>G
NM_000430.3:c.926C>G	NP_000421.1:p.Pro309Arg
XM_011523901.1:c.980C>G	XP_011522203.1:p.Pro327Arg
XM_011523902.1:c.980C>G	XP_011522204.1:p.Pro327Arg
XM_011523903.1:c.980C>G	XP_011522205.1:p.Pro327Arg
XM_011523901.2:c.980C>G	XP_011522203.1:p.Pro327Arg
XM_011523902.3:c.980C>G	XP_011522204.1:p.Pro327Arg
XM_011523903.2:c.980C>G	XP_011522205.1:p.Pro327Arg
XM_017024701.1:c.926C>G	XP_016880190.1:p.Pro309Arg
XM_017024702.2:c.731C>G	XP_016880191.1:p.Pro244Arg
NM_000430.4:c.926C>G MANE Select	NP_000421.1:p.Pro309Arg