Canonical Allele Identifier: CA2243487236

Gene: PAFAH1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2665305_2665307delinsTAA , CM000679.2:g.2665305_2665307delinsTAA	GRCh38
NC_000017.10:g.2568599_2568601delinsTAA , CM000679.1:g.2568599_2568601delinsTAA	GRCh37
NC_000017.9:g.2515349_2515351delinsTAA	NCBI36
NG_009799.1:g.76677_76679delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.33-67_33-65delinsTAA MANE Select	ENSP00000380378.4:n.33-67_33-65delinsTAA
ENST00000674608.1:c.87-67_87-65delinsTAA	ENSP00000501976.1:n.87-67_87-65delinsTAA
ENST00000674717.1:c.-3-1687_-3-1685delinsTAA	ENSP00000501931.1:n.-3-1687_-3-1685delinsTAA
ENST00000675202.1:c.33-67_33-65delinsTAA	ENSP00000502843.1:n.33-67_33-65delinsTAA
ENST00000675331.1:c.33-67_33-65delinsTAA	ENSP00000502031.1:n.33-67_33-65delinsTAA
ENST00000675390.1:c.33-67_33-65delinsTAA	ENSP00000501969.1:n.33-67_33-65delinsTAA
ENST00000675430.1:n.260-67_260-65delinsTAA
ENST00000675621.1:c.33-67_33-65delinsTAA	ENSP00000502117.1:n.33-67_33-65delinsTAA
ENST00000675764.1:c.131-67_131-65delinsTAA	ENSP00000502242.1:n.131-67_131-65delinsTAA
ENST00000676077.1:c.-163-67_-163-65delinsTAA	ENSP00000502507.1:n.-163-67_-163-65delinsTAA
ENST00000676098.1:c.33-67_33-65delinsTAA	ENSP00000502735.1:n.33-67_33-65delinsTAA
ENST00000676188.1:c.33-67_33-65delinsTAA	ENSP00000502577.1:n.33-67_33-65delinsTAA
ENST00000676201.1:n.272-711_272-709delinsTAA
ENST00000676353.1:c.-78-711_-78-709delinsTAA	ENSP00000502737.1:n.-78-711_-78-709delinsTAA
ENST00000676456.1:n.223-711_223-709delinsTAA
ENST00000397195.9:c.33-67_33-65delinsTAA	ENSP00000380378.4:n.33-67_33-65delinsTAA
ENST00000570400.1:c.33-711_33-709delinsTAA	ENSP00000460258.1:n.33-711_33-709delinsTAA
ENST00000572915.6:n.273-1687_273-1685delinsTAA
ENST00000574816.5:n.31-11009_31-11007delinsTAA
ENST00000575477.5:n.620-711_620-709delinsTAA
ENST00000576586.5:c.33-67_33-65delinsTAA	ENSP00000461087.1:n.33-67_33-65delinsTAA
NM_000430.3:c.33-67_33-65delinsTAA	NP_000421.1:n.33-67_33-65delinsTAA
XM_011523901.1:c.87-67_87-65delinsTAA	XP_011522203.1:n.87-67_87-65delinsTAA
XM_011523902.1:c.87-67_87-65delinsTAA	XP_011522204.1:n.87-67_87-65delinsTAA
XM_011523903.1:c.87-67_87-65delinsTAA	XP_011522205.1:n.87-67_87-65delinsTAA
XM_011523904.1:c.87-67_87-65delinsTAA	XP_011522206.1:n.87-67_87-65delinsTAA
XM_011523901.2:c.87-67_87-65delinsTAA	XP_011522203.1:n.87-67_87-65delinsTAA
XM_011523902.3:c.87-67_87-65delinsTAA	XP_011522204.1:n.87-67_87-65delinsTAA
XM_011523903.2:c.87-67_87-65delinsTAA	XP_011522205.1:n.87-67_87-65delinsTAA
XM_017024701.1:c.33-67_33-65delinsTAA	XP_016880190.1:n.33-67_33-65delinsTAA
XM_017024702.2:c.-78-711_-78-709delinsTAA	XP_016880191.1:n.-78-711_-78-709delinsTAA
NM_000430.4:c.33-67_33-65delinsTAA MANE Select	NP_000421.1:n.33-67_33-65delinsTAA