Canonical Allele Identifier: CA2808226766

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2676708_2676710del , CM000679.2:g.2676708_2676710del	GRCh38
NC_000017.10:g.2580002_2580004del , CM000679.1:g.2580002_2580004del	GRCh37
NC_000017.9:g.2526752_2526754del	NCBI36
NG_009799.1:g.88080_88082del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.1002+102_1002+104del MANE Select	ENSP00000380378.4:n.1002+102_1002+104del
ENST00000571495.2:n.2087+102_2087+104del
ENST00000674608.1:c.1056+102_1056+104del	ENSP00000501976.1:n.1056+102_1056+104del
ENST00000674717.1:c.807+102_807+104del	ENSP00000501931.1:n.807+102_807+104del
ENST00000675084.1:n.256+102_256+104del
ENST00000675202.1:c.1002+102_1002+104del	ENSP00000502843.1:n.1002+102_1002+104del
ENST00000675331.1:c.1002+102_1002+104del	ENSP00000502031.1:n.1002+102_1002+104del
ENST00000675385.1:n.616+102_616+104del
ENST00000675390.1:c.1002+102_1002+104del	ENSP00000501969.1:n.1002+102_1002+104del
ENST00000675574.1:n.4057+102_4057+104del
ENST00000675621.1:c.1002+102_1002+104del	ENSP00000502117.1:n.1002+102_1002+104del
ENST00000675764.1:c.*956+102_*956+104del	ENSP00000502242.1:n.*956+102_*956+104del
ENST00000676077.1:c.*320+102_*320+104del	ENSP00000502507.1:n.*320+102_*320+104del
ENST00000676098.1:c.1002+102_1002+104del	ENSP00000502735.1:n.1002+102_1002+104del
ENST00000676188.1:c.1002+102_1002+104del	ENSP00000502577.1:n.1002+102_1002+104del
ENST00000676353.1:c.807+102_807+104del	ENSP00000502737.1:n.807+102_807+104del
ENST00000397193.7:n.810+102_810+104del
ENST00000397195.9:c.1002+102_1002+104del	ENSP00000380378.4:n.1002+102_1002+104del
ENST00000571495.1:n.726+102_726+104del
ENST00000572915.6:n.676+2612_676+2614del
ENST00000574468.1:c.396+2420_396+2422del	ENSP00000460591.1:n.396+2420_396+2422del
ENST00000574816.5:n.323+102_323+104del
NM_000430.3:c.1002+102_1002+104del	NP_000421.1:n.1002+102_1002+104del
XM_011523901.1:c.1056+102_1056+104del	XP_011522203.1:n.1056+102_1056+104del
XM_011523902.1:c.1056+102_1056+104del	XP_011522204.1:n.1056+102_1056+104del
XM_011523903.1:c.1056+102_1056+104del	XP_011522205.1:n.1056+102_1056+104del
XM_011523901.2:c.1056+102_1056+104del	XP_011522203.1:n.1056+102_1056+104del
XM_011523902.3:c.1056+102_1056+104del	XP_011522204.1:n.1056+102_1056+104del
XM_011523903.2:c.1056+102_1056+104del	XP_011522205.1:n.1056+102_1056+104del
XM_017024701.1:c.1002+102_1002+104del	XP_016880190.1:n.1002+102_1002+104del
XM_017024702.2:c.807+102_807+104del	XP_016880191.1:n.807+102_807+104del
NM_000430.4:c.1002+102_1002+104del MANE Select	NP_000421.1:n.1002+102_1002+104del