Canonical Allele Identifier: CA117016441

Gene: NADK2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36211748T>G , CM000667.2:g.36211748T>G	GRCh38
NC_000005.9:g.36211850T>G , CM000667.1:g.36211850T>G	GRCh37
NC_000005.8:g.36247607T>G	NCBI36
NG_041784.1:g.35532A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001085411.3:c.860+96A>C MANE Select	NP_001078880.1:n.860+96A>C
ENST00000381937.9:c.860+96A>C MANE Select	ENSP00000371362.4:n.860+96A>C
NM_001085411.2:c.860+96A>C	NP_001078880.1:n.860+96A>C
NM_001287340.1:c.371+96A>C	NP_001274269.1:n.371+96A>C
NM_001287340.2:c.371+96A>C	NP_001274269.1:n.371+96A>C
NM_001287341.1:c.371+96A>C	NP_001274270.1:n.371+96A>C
NM_001287341.2:c.371+96A>C	NP_001274270.1:n.371+96A>C
NM_153013.4:c.371+96A>C	NP_694558.1:n.371+96A>C
NM_153013.5:c.371+96A>C	NP_694558.1:n.371+96A>C
ENST00000282512.7:c.371+96A>C	ENSP00000282512.3:n.371+96A>C
ENST00000381937.8:c.860+96A>C	ENSP00000371362.4:n.860+96A>C
ENST00000397338.5:c.371+96A>C	ENSP00000380499.1:n.371+96A>C
ENST00000404560.7:n.589+96A>C
ENST00000506945.5:c.371+96A>C	ENSP00000422250.1:n.371+96A>C
ENST00000509225.1:n.230+96A>C
ENST00000511613.5:n.244+96A>C
ENST00000514504.5:c.860+96A>C	ENSP00000421029.1:n.860+96A>C
ENST00000617628.4:c.371+96A>C	ENSP00000480506.1:n.371+96A>C
XM_005248241.3:c.860+96A>C	XP_005248298.1:n.860+96A>C
XM_005248241.4:c.860+96A>C	XP_005248298.1:n.860+96A>C
XM_011513954.1:c.371+96A>C	XP_011512256.1:n.371+96A>C
XM_011513955.1:c.371+96A>C	XP_011512257.1:n.371+96A>C
XM_024454360.1:c.371+96A>C	XP_024310128.1:n.371+96A>C