Canonical Allele Identifier: CA2221842348
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722996T= , CM000678.2:g.50722996T= GRCh38
NC_000016.9:g.50756907T= , CM000678.1:g.50756907T= GRCh37
NC_000016.8:g.49314408T= NCBI36
NG_007508.1:g.30858T= , LRG_177:g.30858T=

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.2382-6822T= ENSP00000493088.1:n.2382-6822T=
ENST00000646677.2:c.*482+291T= ENSP00000496533.1:n.*482+291T=
ENST00000697425.1:c.544+291T=
ENST00000697426.1:c.432+291T=
ENST00000697427.1:c.348+291T=
ENST00000697428.1:n.2195+291T=
ENST00000641284.1:c.2382-6822T= ENSP00000493088.1:n.2382-6822T=
ENST00000646677.1:c.*482+291T= ENSP00000496533.1:n.*482+291T=
ENST00000647318.2:c.2717+291T= MANE Select ENSP00000495993.1:n.2717+291T=
ENST00000300589.6:c.2798+291T= ENSP00000300589.2:n.2798+291T=
ENST00000524712.5:c.292+291T=
ENST00000527052.5:c.264+291T=
ENST00000529633.5:c.376+291T=
ENST00000534057.1:c.432+291T=
ENST00000534067.5:c.528+291T=
NM_001293557.1:c.2717+291T= NP_001280486.1:n.2717+291T=
NM_022162.2:c.2798+291T= NP_071445.1:n.2798+291T=
XM_005256084.2:c.2717+291T= XP_005256141.1:n.2717+291T=
XM_006721242.2:c.2633+291T= XP_006721305.1:n.2633+291T=
XM_011523257.1:c.2294+291T= XP_011521559.1:n.2294+291T=
XM_011523258.1:c.2294+291T= XP_011521560.1:n.2294+291T=
XM_011523259.1:c.2132+291T= XP_011521561.1:n.2132+291T=
XR_429725.2:n.2639+291T=
XR_429726.2:n.2555+291T=
XR_933387.1:n.2835+291T=
XM_005256084.4:c.2717+291T= XP_005256141.1:n.2717+291T=
XM_006721242.4:c.2633+291T= XP_006721305.1:n.2633+291T=
XM_011523259.2:c.2132+291T= XP_011521561.1:n.2132+291T=
XM_017023535.1:c.2225+291T= XP_016879024.1:n.2225+291T=
XM_017023536.1:c.2132+291T= XP_016879025.1:n.2132+291T=
XM_017023537.1:c.2132+291T= XP_016879026.1:n.2132+291T=
XM_017023538.1:c.2132+291T= XP_016879027.1:n.2132+291T=
XR_429725.3:n.2592+291T=
XR_429726.3:n.2508+291T=
XR_933387.2:n.2788+291T=
NM_001293557.2:c.2717+291T= NP_001280486.1:n.2717+291T=
NM_001370466.1:c.2717+291T= MANE Select NP_001357395.1:n.2717+291T=
NM_022162.3:c.2798+291T= NP_071445.1:n.2798+291T=
NR_163434.1:n.2929+291T=