Canonical Allele Identifier: CA395875051
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722637A>C , CM000678.2:g.50722637A>C GRCh38
NC_000016.9:g.50756548A>C , CM000678.1:g.50756548A>C GRCh37
NC_000016.8:g.49314049A>C NCBI36
NG_007508.1:g.30499A>C , LRG_177:g.30499A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.2382-7181A>C ENSP00000493088.1:n.2382-7181A>C
ENST00000646677.2:c.*414A>C ENSP00000496533.1:n.*414A>C
ENST00000697425.1:c.476A>C
ENST00000697426.1:c.364A>C
ENST00000697427.1:c.280A>C
ENST00000697428.1:n.2127A>C
ENST00000641284.1:c.2382-7181A>C ENSP00000493088.1:n.2382-7181A>C
ENST00000646677.1:c.*414A>C ENSP00000496533.1:n.*414A>C
ENST00000647318.2:c.2649A>C MANE Select ENSP00000495993.1:p.Arg883Ser
ENST00000300589.6:c.2730A>C ENSP00000300589.2:p.Arg910Ser
ENST00000524712.5:c.224A>C
ENST00000527052.5:c.196A>C
ENST00000529633.5:c.308A>C
ENST00000534057.1:c.364A>C
ENST00000534067.5:c.460A>C
NM_001293557.1:c.2649A>C NP_001280486.1:p.Arg883Ser
NM_022162.2:c.2730A>C NP_071445.1:p.Arg910Ser
XM_005256084.2:c.2649A>C XP_005256141.1:p.Arg883Ser
XM_006721242.2:c.2565A>C XP_006721305.1:p.Arg855Ser
XM_011523257.1:c.2226A>C XP_011521559.1:p.Arg742Ser
XM_011523258.1:c.2226A>C XP_011521560.1:p.Arg742Ser
XM_011523259.1:c.2064A>C XP_011521561.1:p.Arg688Ser
XR_429725.2:n.2571A>C
XR_429726.2:n.2487A>C
XR_933387.1:n.2767A>C
XM_005256084.4:c.2649A>C XP_005256141.1:p.Arg883Ser
XM_006721242.4:c.2565A>C XP_006721305.1:p.Arg855Ser
XM_011523259.2:c.2064A>C XP_011521561.1:p.Arg688Ser
XM_017023535.1:c.2157A>C XP_016879024.1:p.Arg719Ser
XM_017023536.1:c.2064A>C XP_016879025.1:p.Arg688Ser
XM_017023537.1:c.2064A>C XP_016879026.1:p.Arg688Ser
XM_017023538.1:c.2064A>C XP_016879027.1:p.Arg688Ser
XR_429725.3:n.2524A>C
XR_429726.3:n.2440A>C
XR_933387.2:n.2720A>C
NM_001293557.2:c.2649A>C NP_001280486.1:p.Arg883Ser
NM_001370466.1:c.2649A>C MANE Select NP_001357395.1:p.Arg883Ser
NM_022162.3:c.2730A>C NP_071445.1:p.Arg910Ser
NR_163434.1:n.2861A>C