Canonical Allele Identifier: CA397642213
Gene: PAFAH1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2676548C>G , CM000679.2:g.2676548C>G GRCh38
NC_000017.10:g.2579842C>G , CM000679.1:g.2579842C>G GRCh37
NC_000017.9:g.2526592C>G NCBI36
NG_009799.1:g.87920C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.944C>G MANE Select ENSP00000380378.4:p.Ser315Cys
ENST00000571495.2:n.2029C>G
ENST00000674608.1:c.998C>G ENSP00000501976.1:p.Ser333Cys
ENST00000674717.1:c.749C>G ENSP00000501931.1:p.Ser250Cys
ENST00000675084.1:n.198C>G
ENST00000675202.1:c.944C>G ENSP00000502843.1:p.Ser315Cys
ENST00000675331.1:c.944C>G ENSP00000502031.1:p.Ser315Cys
ENST00000675385.1:n.558C>G
ENST00000675390.1:c.944C>G ENSP00000501969.1:p.Ser315Cys
ENST00000675574.1:n.3999C>G
ENST00000675621.1:c.944C>G ENSP00000502117.1:p.Ser315Cys
ENST00000675764.1:c.*898C>G ENSP00000502242.1:n.*898C>G
ENST00000676077.1:c.*262C>G ENSP00000502507.1:n.*262C>G
ENST00000676098.1:c.944C>G ENSP00000502735.1:p.Ser315Cys
ENST00000676188.1:c.944C>G ENSP00000502577.1:p.Ser315Cys
ENST00000676353.1:c.749C>G ENSP00000502737.1:p.Ser250Cys
ENST00000397193.7:n.752C>G
ENST00000397195.9:c.944C>G ENSP00000380378.4:p.Ser315Cys
ENST00000571495.1:n.668C>G
ENST00000572915.6:n.676+2452C>G
ENST00000574468.1:c.396+2260C>G ENSP00000460591.1:n.396+2260C>G
ENST00000574816.5:n.265C>G
NM_000430.3:c.944C>G NP_000421.1:p.Ser315Cys
XM_011523901.1:c.998C>G XP_011522203.1:p.Ser333Cys
XM_011523902.1:c.998C>G XP_011522204.1:p.Ser333Cys
XM_011523903.1:c.998C>G XP_011522205.1:p.Ser333Cys
XM_011523901.2:c.998C>G XP_011522203.1:p.Ser333Cys
XM_011523902.3:c.998C>G XP_011522204.1:p.Ser333Cys
XM_011523903.2:c.998C>G XP_011522205.1:p.Ser333Cys
XM_017024701.1:c.944C>G XP_016880190.1:p.Ser315Cys
XM_017024702.2:c.749C>G XP_016880191.1:p.Ser250Cys
NM_000430.4:c.944C>G MANE Select NP_000421.1:p.Ser315Cys