Canonical Allele Identifier: CA6371932

Gene: NCAPD3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134209361T>C , CM000673.2:g.134209361T>C	GRCh38
NC_000011.9:g.134079255T>C , CM000673.1:g.134079255T>C	GRCh37
NC_000011.8:g.133584465T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015261.3:c.684A>G MANE Select	NP_056076.1:p.Pro228=
ENST00000534548.7:c.684A>G MANE Select	ENSP00000433681.3:p.Pro228=
NM_001372065.1:c.684A>G	NP_001358994.1:p.Pro228=
NM_001372068.1:c.684A>G	NP_001358997.1:p.Pro228=
NM_001372069.1:c.270A>G	NP_001358998.1:p.Pro90=
NM_001372070.1:c.270A>G	NP_001358999.1:p.Pro90=
NM_015261.2:c.684A>G	NP_056076.1:p.Pro228=
ENST00000525432.2:n.705A>G
ENST00000525964.6:c.684A>G	ENSP00000431612.2:p.Pro228=
ENST00000525964.7:c.684A>G	ENSP00000431612.2:p.Pro228=
ENST00000528065.1:n.374A>G
ENST00000533155.5:c.*293A>G	ENSP00000431413.1:n.*293A>G
ENST00000533155.6:c.309A>G
ENST00000534532.6:c.684A>G	ENSP00000434168.2:p.Pro228=
ENST00000534532.7:c.684A>G	ENSP00000434168.2:p.Pro228=
ENST00000534548.6:c.684A>G	ENSP00000433681.2:p.Pro228=
ENST00000685324.1:c.684A>G	ENSP00000508707.1:p.Pro228=
ENST00000687155.1:n.744A>G
ENST00000687480.1:n.740A>G
ENST00000687965.1:c.302A>G
ENST00000688263.1:c.684A>G	ENSP00000510008.1:p.Pro228=
ENST00000688672.1:c.684A>G	ENSP00000510391.1:p.Pro228=
ENST00000689205.1:c.*386A>G	ENSP00000510550.1:n.*386A>G
ENST00000690149.1:c.302A>G
ENST00000690743.1:c.*293A>G	ENSP00000508701.1:n.*293A>G
ENST00000692494.1:n.726A>G
ENST00000693663.1:n.1311A>G
XM_011542718.1:c.684A>G	XP_011541020.1:p.Pro228=
XM_011542719.1:c.270A>G	XP_011541021.1:p.Pro90=
XM_011542719.2:c.270A>G	XP_011541021.1:p.Pro90=
XM_024448406.1:c.684A>G	XP_024304174.1:p.Pro228=
XM_024448407.1:c.684A>G	XP_024304175.1:p.Pro228=
XR_001747803.2:n.1116A>G
XR_947815.1:n.1007A>G
XR_947815.3:n.1116A>G
XR_947816.1:n.1007A>G