Canonical Allele Identifier: CA6371536

Gene: NCAPD3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.134194113C>T , CM000673.2:g.134194113C>T	GRCh38
NC_000011.9:g.134064008C>T , CM000673.1:g.134064008C>T	GRCh37
NC_000011.8:g.133569218C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015261.3:c.1727G>A MANE Select	NP_056076.1:p.Gly576Asp
ENST00000534548.7:c.1727G>A MANE Select	ENSP00000433681.3:p.Gly576Asp
NM_001372065.1:c.1727G>A	NP_001358994.1:p.Gly576Asp
NM_001372068.1:c.1727G>A	NP_001358997.1:p.Gly576Asp
NM_001372069.1:c.1313G>A	NP_001358998.1:p.Gly438Asp
NM_001372070.1:c.1313G>A	NP_001358999.1:p.Gly438Asp
NM_015261.2:c.1727G>A	NP_056076.1:p.Gly576Asp
ENST00000525432.2:n.1748G>A
ENST00000525964.6:c.1727G>A	ENSP00000431612.2:p.Gly576Asp
ENST00000525964.7:c.1727G>A	ENSP00000431612.2:p.Gly576Asp
ENST00000534532.6:c.1727G>A	ENSP00000434168.2:p.Gly576Asp
ENST00000534532.7:c.1727G>A	ENSP00000434168.2:p.Gly576Asp
ENST00000534548.6:c.1727G>A	ENSP00000433681.2:p.Gly576Asp
ENST00000685119.1:n.726G>A
ENST00000685324.1:c.1727G>A	ENSP00000508707.1:p.Gly576Asp
ENST00000687155.1:n.1787G>A
ENST00000687480.1:n.2234G>A
ENST00000688263.1:c.1727G>A	ENSP00000510008.1:p.Gly576Asp
ENST00000688672.1:c.1727G>A	ENSP00000510391.1:p.Gly576Asp
ENST00000689205.1:c.*1429G>A	ENSP00000510550.1:n.*1429G>A
ENST00000689387.1:c.929G>A
ENST00000690149.1:c.1283G>A
ENST00000690743.1:c.*1336G>A	ENSP00000508701.1:n.*1336G>A
ENST00000692494.1:n.1769G>A
XM_011542718.1:c.1727G>A	XP_011541020.1:p.Gly576Asp
XM_011542719.1:c.1313G>A	XP_011541021.1:p.Gly438Asp
XM_011542719.2:c.1313G>A	XP_011541021.1:p.Gly438Asp
XM_024448406.1:c.1727G>A	XP_024304174.1:p.Gly576Asp
XM_024448407.1:c.1727G>A	XP_024304175.1:p.Gly576Asp
XR_001747803.2:n.2159G>A
XR_947815.1:n.2050G>A
XR_947815.3:n.2159G>A
XR_947816.1:n.2050G>A