Canonical Allele Identifier: CA2635351476
Gene: PAFAH1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2676359del , CM000679.2:g.2676359del GRCh38
NC_000017.10:g.2579653del , CM000679.1:g.2579653del GRCh37
NC_000017.9:g.2526403del NCBI36
NG_009799.1:g.87731del

Transcript Alleles

HGVS Amino-acid Change
ENST00000397195.10:c.901-146del MANE Select ENSP00000380378.4:n.901-146del
ENST00000571495.2:n.1986-146del
ENST00000674608.1:c.955-146del ENSP00000501976.1:n.955-146del
ENST00000674717.1:c.706-146del ENSP00000501931.1:n.706-146del
ENST00000675084.1:n.9del
ENST00000675202.1:c.901-146del ENSP00000502843.1:n.901-146del
ENST00000675331.1:c.901-146del ENSP00000502031.1:n.901-146del
ENST00000675385.1:n.369del
ENST00000675390.1:c.901-146del ENSP00000501969.1:n.901-146del
ENST00000675574.1:n.3810del
ENST00000675621.1:c.901-146del ENSP00000502117.1:n.901-146del
ENST00000675764.1:c.*855-146del ENSP00000502242.1:n.*855-146del
ENST00000676077.1:c.*219-146del ENSP00000502507.1:n.*219-146del
ENST00000676098.1:c.901-146del ENSP00000502735.1:n.901-146del
ENST00000676188.1:c.901-146del ENSP00000502577.1:n.901-146del
ENST00000676353.1:c.706-146del ENSP00000502737.1:n.706-146del
ENST00000397193.7:n.709-146del
ENST00000397195.9:c.901-146del ENSP00000380378.4:n.901-146del
ENST00000571495.1:n.625-146del
ENST00000572915.6:n.676+2263del
ENST00000574468.1:c.396+2071del ENSP00000460591.1:n.396+2071del
ENST00000574816.5:n.76del
NM_000430.3:c.901-146del NP_000421.1:n.901-146del
XM_011523901.1:c.955-146del XP_011522203.1:n.955-146del
XM_011523902.1:c.955-146del XP_011522204.1:n.955-146del
XM_011523903.1:c.955-146del XP_011522205.1:n.955-146del
XM_011523901.2:c.955-146del XP_011522203.1:n.955-146del
XM_011523902.3:c.955-146del XP_011522204.1:n.955-146del
XM_011523903.2:c.955-146del XP_011522205.1:n.955-146del
XM_017024701.1:c.901-146del XP_016880190.1:n.901-146del
XM_017024702.2:c.706-146del XP_016880191.1:n.706-146del
NM_000430.4:c.901-146del MANE Select NP_000421.1:n.901-146del