Canonical Allele Identifier: CA277002
Gene: PAFAH1B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 211823
ClinVar RCV Id: RCV000192650
dbSNP Id: rs797045859

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2667146dup , CM000679.2:g.2667146dup GRCh38
NC_000017.10:g.2570440dup , CM000679.1:g.2570440dup GRCh37
NC_000017.9:g.2517190dup NCBI36
NG_009799.1:g.78518dup

Transcript Alleles

HGVS Amino-acid change
ENST00000397195.10:c.347dup MANE Select ENSP00000380378.4:p.His117ProfsTer17
ENST00000674608.1:c.401dup ENSP00000501976.1:p.His135ProfsTer17
ENST00000674717.1:c.152dup ENSP00000501931.1:p.His52ProfsTer17
ENST00000675202.1:c.347dup ENSP00000502843.1:p.His117ProfsTer17
ENST00000675331.1:c.347dup ENSP00000502031.1:p.His117ProfsTer17
ENST00000675390.1:c.347dup ENSP00000501969.1:p.His117ProfsTer17
ENST00000675430.1:n.574dup
ENST00000675621.1:c.347dup ENSP00000502117.1:p.His117ProfsTer17
ENST00000675764.1:c.*301dup ENSP00000502242.1:n.*301dup
ENST00000676077.1:c.152dup ENSP00000502507.1:p.His52ProfsTer17
ENST00000676098.1:c.347dup ENSP00000502735.1:p.His117ProfsTer17
ENST00000676188.1:c.347dup ENSP00000502577.1:p.His117ProfsTer17
ENST00000676201.1:n.501dup
ENST00000676353.1:c.152dup ENSP00000502737.1:p.His52ProfsTer17
ENST00000676456.1:n.452dup
ENST00000397195.9:c.347dup ENSP00000380378.4:p.His117ProfsTer17
ENST00000570400.1:c.*217dup ENSP00000460258.1:n.*217dup
ENST00000572915.6:n.427dup
ENST00000574816.5:n.31-9168dup
ENST00000609078.1:n.306dup
NM_000430.3:c.347dup NP_000421.1:p.His117ProfsTer17
XM_011523901.1:c.401dup XP_011522203.1:p.His135ProfsTer17
XM_011523902.1:c.401dup XP_011522204.1:p.His135ProfsTer17
XM_011523903.1:c.401dup XP_011522205.1:p.His135ProfsTer17
XM_011523904.1:c.401dup XP_011522206.1:p.His135ProfsTer17
XM_011523901.2:c.401dup XP_011522203.1:p.His135ProfsTer17
XM_011523902.3:c.401dup XP_011522204.1:p.His135ProfsTer17
XM_011523903.2:c.401dup XP_011522205.1:p.His135ProfsTer17
XM_017024701.1:c.347dup XP_016880190.1:p.His117ProfsTer17
XM_017024702.2:c.152dup XP_016880191.1:p.His52ProfsTer17
NM_000430.4:c.347dup MANE Select NP_000421.1:p.His117ProfsTer17