Canonical Allele Identifier: CA2807003258

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50732878A>G , CM000678.2:g.50732878A>G	GRCh38
NC_000016.9:g.50766789A>G , CM000678.1:g.50766789A>G	GRCh37
NC_000016.8:g.49324290A>G	NCBI36
NG_007508.1:g.40740A>G , LRG_177:g.40740A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.*1215A>G	ENSP00000493088.1:n.*1215A>G
ENST00000646677.2:c.*1866A>G	ENSP00000496533.1:n.*1866A>G
ENST00000697428.1:n.3579A>G
ENST00000641284.1:c.*1215A>G	ENSP00000493088.1:n.*1215A>G
ENST00000646677.1:c.*1866A>G	ENSP00000496533.1:n.*1866A>G
ENST00000647318.2:c.*1059A>G MANE Select	ENSP00000495993.1:n.*1059A>G
ENST00000300589.6:c.*1059A>G	ENSP00000300589.2:n.*1059A>G
NM_001293557.1:c.*1059A>G	NP_001280486.1:n.*1059A>G
NM_022162.2:c.*1059A>G	NP_071445.1:n.*1059A>G
XM_005256084.2:c.*1059A>G	XP_005256141.1:n.*1059A>G
XM_006721242.2:c.*1059A>G	XP_006721305.1:n.*1059A>G
XM_011523257.1:c.*1059A>G	XP_011521559.1:n.*1059A>G
XM_011523258.1:c.*1059A>G	XP_011521560.1:n.*1059A>G
XM_011523259.1:c.*1059A>G	XP_011521561.1:n.*1059A>G
XM_005256084.4:c.*1059A>G	XP_005256141.1:n.*1059A>G
XM_006721242.4:c.*1059A>G	XP_006721305.1:n.*1059A>G
XM_011523259.2:c.*1059A>G	XP_011521561.1:n.*1059A>G
XM_017023535.1:c.*1059A>G	XP_016879024.1:n.*1059A>G
XM_017023536.1:c.*1059A>G	XP_016879025.1:n.*1059A>G
XM_017023537.1:c.*1059A>G	XP_016879026.1:n.*1059A>G
XM_017023538.1:c.*1059A>G	XP_016879027.1:n.*1059A>G
NM_001293557.2:c.*1059A>G	NP_001280486.1:n.*1059A>G
NM_001370466.1:c.*1059A>G MANE Select	NP_001357395.1:n.*1059A>G
NM_022162.3:c.*1059A>G	NP_071445.1:n.*1059A>G
NR_163434.1:n.4313A>G