Canonical Allele Identifier: CA56387819

Gene: NCKAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.132989057A>T , CM000664.2:g.132989057A>T	GRCh38
NC_000002.11:g.133746630A>T , CM000664.1:g.133746630A>T	GRCh37
NC_000002.10:g.133463100A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409261.6:c.429+5095T>A MANE Select	ENSP00000387128.1:n.429+5095T>A
ENST00000317721.10:c.429+5095T>A	ENSP00000380603.4:n.429+5095T>A
ENST00000405974.7:c.429+5095T>A	ENSP00000385692.4:n.429+5095T>A
ENST00000409213.5:c.429+5095T>A	ENSP00000386952.1:n.429+5095T>A
ENST00000409261.5:c.429+5095T>A	ENSP00000387128.1:n.429+5095T>A
NM_207363.2:c.429+5095T>A	NP_997246.2:n.429+5095T>A
NM_207481.3:c.429+5095T>A	NP_997364.3:n.429+5095T>A
XM_005263659.2:c.429+5095T>A	XP_005263716.1:n.429+5095T>A
XM_005263660.2:c.429+5095T>A	XP_005263717.1:n.429+5095T>A
XM_006712490.2:c.429+5095T>A	XP_006712553.1:n.429+5095T>A
XM_011511097.1:c.429+5095T>A	XP_011509399.1:n.429+5095T>A
XM_011511098.1:c.429+5095T>A	XP_011509400.1:n.429+5095T>A
XM_011511099.1:c.429+5095T>A	XP_011509401.1:n.429+5095T>A
XM_011511100.1:c.429+5095T>A	XP_011509402.1:n.429+5095T>A
XM_011511101.1:c.354+5095T>A	XP_011509403.1:n.354+5095T>A
XM_011511102.1:c.354+5095T>A	XP_011509404.1:n.354+5095T>A
XM_011511103.1:c.225+5095T>A	XP_011509405.1:n.225+5095T>A
XM_011511104.1:c.225+5095T>A	XP_011509406.1:n.225+5095T>A
XM_011511105.1:c.225+5095T>A	XP_011509407.1:n.225+5095T>A
XM_011511106.1:c.117+5095T>A	XP_011509408.1:n.117+5095T>A
XM_005263659.4:c.429+5095T>A	XP_005263716.1:n.429+5095T>A
XM_005263660.4:c.429+5095T>A	XP_005263717.1:n.429+5095T>A
XM_011511097.3:c.429+5095T>A	XP_011509399.1:n.429+5095T>A
XM_011511099.3:c.429+5095T>A	XP_011509401.1:n.429+5095T>A
XM_011511100.3:c.429+5095T>A	XP_011509402.1:n.429+5095T>A
XM_011511102.2:c.354+5095T>A	XP_011509404.1:n.354+5095T>A
XM_011511103.2:c.225+5095T>A	XP_011509405.1:n.225+5095T>A
XM_011511105.2:c.225+5095T>A	XP_011509407.1:n.225+5095T>A
XM_017003974.1:c.429+5095T>A	XP_016859463.1:n.429+5095T>A
XM_017003975.2:c.429+5095T>A	XP_016859464.1:n.429+5095T>A
XM_017003976.2:c.354+5095T>A	XP_016859465.1:n.354+5095T>A
XM_017003977.2:c.354+5095T>A	XP_016859466.1:n.354+5095T>A
XM_017003979.2:c.429+5095T>A	XP_016859468.1:n.429+5095T>A
XM_017003980.1:c.225+5095T>A	XP_016859469.1:n.225+5095T>A
NM_207363.3:c.429+5095T>A MANE Select	NP_997246.2:n.429+5095T>A
NM_207481.4:c.429+5095T>A	NP_997364.3:n.429+5095T>A