Canonical Allele Identifier: CA397642147
Gene: PAFAH1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2676517G>A , CM000679.2:g.2676517G>A GRCh38
NC_000017.10:g.2579811G>A , CM000679.1:g.2579811G>A GRCh37
NC_000017.9:g.2526561G>A NCBI36
NG_009799.1:g.87889G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.913G>A MANE Select ENSP00000380378.4:p.Gly305Ser
ENST00000571495.2:n.1998G>A
ENST00000674608.1:c.967G>A ENSP00000501976.1:p.Gly323Ser
ENST00000674717.1:c.718G>A ENSP00000501931.1:p.Gly240Ser
ENST00000675084.1:n.167G>A
ENST00000675202.1:c.913G>A ENSP00000502843.1:p.Gly305Ser
ENST00000675331.1:c.913G>A ENSP00000502031.1:p.Gly305Ser
ENST00000675385.1:n.527G>A
ENST00000675390.1:c.913G>A ENSP00000501969.1:p.Gly305Ser
ENST00000675574.1:n.3968G>A
ENST00000675621.1:c.913G>A ENSP00000502117.1:p.Gly305Ser
ENST00000675764.1:c.*867G>A ENSP00000502242.1:n.*867G>A
ENST00000676077.1:c.*231G>A ENSP00000502507.1:n.*231G>A
ENST00000676098.1:c.913G>A ENSP00000502735.1:p.Gly305Ser
ENST00000676188.1:c.913G>A ENSP00000502577.1:p.Gly305Ser
ENST00000676353.1:c.718G>A ENSP00000502737.1:p.Gly240Ser
ENST00000397193.7:n.721G>A
ENST00000397195.9:c.913G>A ENSP00000380378.4:p.Gly305Ser
ENST00000571495.1:n.637G>A
ENST00000572915.6:n.676+2421G>A
ENST00000574468.1:c.396+2229G>A ENSP00000460591.1:n.396+2229G>A
ENST00000574816.5:n.234G>A
NM_000430.3:c.913G>A NP_000421.1:p.Gly305Ser
XM_011523901.1:c.967G>A XP_011522203.1:p.Gly323Ser
XM_011523902.1:c.967G>A XP_011522204.1:p.Gly323Ser
XM_011523903.1:c.967G>A XP_011522205.1:p.Gly323Ser
XM_011523901.2:c.967G>A XP_011522203.1:p.Gly323Ser
XM_011523902.3:c.967G>A XP_011522204.1:p.Gly323Ser
XM_011523903.2:c.967G>A XP_011522205.1:p.Gly323Ser
XM_017024701.1:c.913G>A XP_016880190.1:p.Gly305Ser
XM_017024702.2:c.718G>A XP_016880191.1:p.Gly240Ser
NM_000430.4:c.913G>A MANE Select NP_000421.1:p.Gly305Ser