Canonical Allele Identifier: CA2221841747

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722741_50722742delinsGA , CM000678.2:g.50722741_50722742delinsGA	GRCh38
NC_000016.9:g.50756652_50756653delinsGA , CM000678.1:g.50756652_50756653delinsGA	GRCh37
NC_000016.8:g.49314153_49314154delinsGA	NCBI36
NG_007508.1:g.30603_30604delinsGA , LRG_177:g.30603_30604delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7077_2382-7076delinsGA	ENSP00000493088.1:n.2382-7077_2382-7076delinsGA
ENST00000646677.2:c.*482+36_*482+37delinsGA	ENSP00000496533.1:n.*482+36_*482+37delinsGA
ENST00000697425.1:c.544+36_544+37delinsGA
ENST00000697426.1:c.432+36_432+37delinsGA
ENST00000697427.1:c.348+36_348+37delinsGA
ENST00000697428.1:n.2195+36_2195+37delinsGA
ENST00000641284.1:c.2382-7077_2382-7076delinsGA	ENSP00000493088.1:n.2382-7077_2382-7076delinsGA
ENST00000646677.1:c.*482+36_*482+37delinsGA	ENSP00000496533.1:n.*482+36_*482+37delinsGA
ENST00000647318.2:c.2717+36_2717+37delinsGA MANE Select	ENSP00000495993.1:n.2717+36_2717+37delinsGA
ENST00000300589.6:c.2798+36_2798+37delinsGA	ENSP00000300589.2:n.2798+36_2798+37delinsGA
ENST00000524712.5:c.292+36_292+37delinsGA
ENST00000527052.5:c.264+36_264+37delinsGA
ENST00000529633.5:c.376+36_376+37delinsGA
ENST00000534057.1:c.432+36_432+37delinsGA
ENST00000534067.5:c.528+36_528+37delinsGA
NM_001293557.1:c.2717+36_2717+37delinsGA	NP_001280486.1:n.2717+36_2717+37delinsGA
NM_022162.2:c.2798+36_2798+37delinsGA	NP_071445.1:n.2798+36_2798+37delinsGA
XM_005256084.2:c.2717+36_2717+37delinsGA	XP_005256141.1:n.2717+36_2717+37delinsGA
XM_006721242.2:c.2633+36_2633+37delinsGA	XP_006721305.1:n.2633+36_2633+37delinsGA
XM_011523257.1:c.2294+36_2294+37delinsGA	XP_011521559.1:n.2294+36_2294+37delinsGA
XM_011523258.1:c.2294+36_2294+37delinsGA	XP_011521560.1:n.2294+36_2294+37delinsGA
XM_011523259.1:c.2132+36_2132+37delinsGA	XP_011521561.1:n.2132+36_2132+37delinsGA
XR_429725.2:n.2639+36_2639+37delinsGA
XR_429726.2:n.2555+36_2555+37delinsGA
XR_933387.1:n.2835+36_2835+37delinsGA
XM_005256084.4:c.2717+36_2717+37delinsGA	XP_005256141.1:n.2717+36_2717+37delinsGA
XM_006721242.4:c.2633+36_2633+37delinsGA	XP_006721305.1:n.2633+36_2633+37delinsGA
XM_011523259.2:c.2132+36_2132+37delinsGA	XP_011521561.1:n.2132+36_2132+37delinsGA
XM_017023535.1:c.2225+36_2225+37delinsGA	XP_016879024.1:n.2225+36_2225+37delinsGA
XM_017023536.1:c.2132+36_2132+37delinsGA	XP_016879025.1:n.2132+36_2132+37delinsGA
XM_017023537.1:c.2132+36_2132+37delinsGA	XP_016879026.1:n.2132+36_2132+37delinsGA
XM_017023538.1:c.2132+36_2132+37delinsGA	XP_016879027.1:n.2132+36_2132+37delinsGA
XR_429725.3:n.2592+36_2592+37delinsGA
XR_429726.3:n.2508+36_2508+37delinsGA
XR_933387.2:n.2788+36_2788+37delinsGA
NM_001293557.2:c.2717+36_2717+37delinsGA	NP_001280486.1:n.2717+36_2717+37delinsGA
NM_001370466.1:c.2717+36_2717+37delinsGA MANE Select	NP_001357395.1:n.2717+36_2717+37delinsGA
NM_022162.3:c.2798+36_2798+37delinsGA	NP_071445.1:n.2798+36_2798+37delinsGA
NR_163434.1:n.2929+36_2929+37delinsGA