Canonical Allele Identifier: CA56418778

Gene: NCKAP5

Linked Data

• dbSNP Id: rs976283198
• MyVariant Identifiers: chr2:g.134017054C>T (hg19) ; chr2:g.133259482C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.133259482C>T , CM000664.2:g.133259482C>T	GRCh38
NC_000002.11:g.134017054C>T , CM000664.1:g.134017054C>T	GRCh37
NC_000002.10:g.133733524C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000409261.6:c.143+43555G>A MANE Select	ENSP00000387128.1:n.143+43555G>A
ENST00000317721.10:c.143+43555G>A	ENSP00000380603.4:n.143+43555G>A
ENST00000358991.4:c.143+43555G>A	ENSP00000351882.4:n.143+43555G>A
ENST00000405974.7:c.143+43555G>A	ENSP00000385692.4:n.143+43555G>A
ENST00000409213.5:c.143+43555G>A	ENSP00000386952.1:n.143+43555G>A
ENST00000409261.5:c.143+43555G>A	ENSP00000387128.1:n.143+43555G>A
ENST00000427594.5:c.130+43555G>A
NM_207363.2:c.143+43555G>A	NP_997246.2:n.143+43555G>A
NM_207481.3:c.143+43555G>A	NP_997364.3:n.143+43555G>A
XM_005263659.2:c.143+43555G>A	XP_005263716.1:n.143+43555G>A
XM_005263660.2:c.143+43555G>A	XP_005263717.1:n.143+43555G>A
XM_006712490.2:c.143+43555G>A	XP_006712553.1:n.143+43555G>A
XM_011511097.1:c.143+43555G>A	XP_011509399.1:n.143+43555G>A
XM_011511098.1:c.143+43555G>A	XP_011509400.1:n.143+43555G>A
XM_011511099.1:c.143+43555G>A	XP_011509401.1:n.143+43555G>A
XM_011511100.1:c.143+43555G>A	XP_011509402.1:n.143+43555G>A
XM_011511101.1:c.68+43555G>A	XP_011509403.1:n.68+43555G>A
XM_011511102.1:c.68+43555G>A	XP_011509404.1:n.68+43555G>A
XM_011511103.1:c.-62+7031G>A	XP_011509405.1:n.-62+7031G>A
XM_011511104.1:c.-61-45703G>A	XP_011509406.1:n.-61-45703G>A
XM_005263659.4:c.143+43555G>A	XP_005263716.1:n.143+43555G>A
XM_005263660.4:c.143+43555G>A	XP_005263717.1:n.143+43555G>A
XM_011511097.3:c.143+43555G>A	XP_011509399.1:n.143+43555G>A
XM_011511099.3:c.143+43555G>A	XP_011509401.1:n.143+43555G>A
XM_011511100.3:c.143+43555G>A	XP_011509402.1:n.143+43555G>A
XM_011511102.2:c.68+43555G>A	XP_011509404.1:n.68+43555G>A
XM_011511103.2:c.-62+7031G>A	XP_011509405.1:n.-62+7031G>A
XM_017003974.1:c.143+43555G>A	XP_016859463.1:n.143+43555G>A
XM_017003975.2:c.143+43555G>A	XP_016859464.1:n.143+43555G>A
XM_017003976.2:c.68+43555G>A	XP_016859465.1:n.68+43555G>A
XM_017003977.2:c.68+43555G>A	XP_016859466.1:n.68+43555G>A
XM_017003979.2:c.143+43555G>A	XP_016859468.1:n.143+43555G>A
XM_017003980.1:c.-62+7031G>A	XP_016859469.1:n.-62+7031G>A
NM_207363.3:c.143+43555G>A MANE Select	NP_997246.2:n.143+43555G>A
NM_207481.4:c.143+43555G>A	NP_997364.3:n.143+43555G>A