Canonical Allele Identifier: CA2221841793

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722746_50722754delinsCAGGTGAAG , CM000678.2:g.50722746_50722754delinsCAGGTGAAG	GRCh38
NC_000016.9:g.50756657_50756665delinsCAGGTGAAG , CM000678.1:g.50756657_50756665delinsCAGGTGAAG	GRCh37
NC_000016.8:g.49314158_49314166delinsCAGGTGAAG	NCBI36
NG_007508.1:g.30608_30616delinsCAGGTGAAG , LRG_177:g.30608_30616delinsCAGGTGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7072_2382-7064delinsCAGGTGAAG	ENSP00000493088.1:n.2382-7072_2382-7064delinsCAGGTGAAG
ENST00000646677.2:c.*482+41_*482+49delinsCAGGTGAAG	ENSP00000496533.1:n.*482+41_*482+49delinsCAGGTGAAG
ENST00000697425.1:c.544+41_544+49delinsCAGGTGAAG
ENST00000697426.1:c.432+41_432+49delinsCAGGTGAAG
ENST00000697427.1:c.348+41_348+49delinsCAGGTGAAG
ENST00000697428.1:n.2195+41_2195+49delinsCAGGTGAAG
ENST00000641284.1:c.2382-7072_2382-7064delinsCAGGTGAAG	ENSP00000493088.1:n.2382-7072_2382-7064delinsCAGGTGAAG
ENST00000646677.1:c.*482+41_*482+49delinsCAGGTGAAG	ENSP00000496533.1:n.*482+41_*482+49delinsCAGGTGAAG
ENST00000647318.2:c.2717+41_2717+49delinsCAGGTGAAG MANE Select	ENSP00000495993.1:n.2717+41_2717+49delinsCAGGTGAAG
ENST00000300589.6:c.2798+41_2798+49delinsCAGGTGAAG	ENSP00000300589.2:n.2798+41_2798+49delinsCAGGTGAAG
ENST00000524712.5:c.292+41_292+49delinsCAGGTGAAG
ENST00000527052.5:c.264+41_264+49delinsCAGGTGAAG
ENST00000529633.5:c.376+41_376+49delinsCAGGTGAAG
ENST00000534057.1:c.432+41_432+49delinsCAGGTGAAG
ENST00000534067.5:c.528+41_528+49delinsCAGGTGAAG
NM_001293557.1:c.2717+41_2717+49delinsCAGGTGAAG	NP_001280486.1:n.2717+41_2717+49delinsCAGGTGAAG
NM_022162.2:c.2798+41_2798+49delinsCAGGTGAAG	NP_071445.1:n.2798+41_2798+49delinsCAGGTGAAG
XM_005256084.2:c.2717+41_2717+49delinsCAGGTGAAG	XP_005256141.1:n.2717+41_2717+49delinsCAGGTGAAG
XM_006721242.2:c.2633+41_2633+49delinsCAGGTGAAG	XP_006721305.1:n.2633+41_2633+49delinsCAGGTGAAG
XM_011523257.1:c.2294+41_2294+49delinsCAGGTGAAG	XP_011521559.1:n.2294+41_2294+49delinsCAGGTGAAG
XM_011523258.1:c.2294+41_2294+49delinsCAGGTGAAG	XP_011521560.1:n.2294+41_2294+49delinsCAGGTGAAG
XM_011523259.1:c.2132+41_2132+49delinsCAGGTGAAG	XP_011521561.1:n.2132+41_2132+49delinsCAGGTGAAG
XR_429725.2:n.2639+41_2639+49delinsCAGGTGAAG
XR_429726.2:n.2555+41_2555+49delinsCAGGTGAAG
XR_933387.1:n.2835+41_2835+49delinsCAGGTGAAG
XM_005256084.4:c.2717+41_2717+49delinsCAGGTGAAG	XP_005256141.1:n.2717+41_2717+49delinsCAGGTGAAG
XM_006721242.4:c.2633+41_2633+49delinsCAGGTGAAG	XP_006721305.1:n.2633+41_2633+49delinsCAGGTGAAG
XM_011523259.2:c.2132+41_2132+49delinsCAGGTGAAG	XP_011521561.1:n.2132+41_2132+49delinsCAGGTGAAG
XM_017023535.1:c.2225+41_2225+49delinsCAGGTGAAG	XP_016879024.1:n.2225+41_2225+49delinsCAGGTGAAG
XM_017023536.1:c.2132+41_2132+49delinsCAGGTGAAG	XP_016879025.1:n.2132+41_2132+49delinsCAGGTGAAG
XM_017023537.1:c.2132+41_2132+49delinsCAGGTGAAG	XP_016879026.1:n.2132+41_2132+49delinsCAGGTGAAG
XM_017023538.1:c.2132+41_2132+49delinsCAGGTGAAG	XP_016879027.1:n.2132+41_2132+49delinsCAGGTGAAG
XR_429725.3:n.2592+41_2592+49delinsCAGGTGAAG
XR_429726.3:n.2508+41_2508+49delinsCAGGTGAAG
XR_933387.2:n.2788+41_2788+49delinsCAGGTGAAG
NM_001293557.2:c.2717+41_2717+49delinsCAGGTGAAG	NP_001280486.1:n.2717+41_2717+49delinsCAGGTGAAG
NM_001370466.1:c.2717+41_2717+49delinsCAGGTGAAG MANE Select	NP_001357395.1:n.2717+41_2717+49delinsCAGGTGAAG
NM_022162.3:c.2798+41_2798+49delinsCAGGTGAAG	NP_071445.1:n.2798+41_2798+49delinsCAGGTGAAG
NR_163434.1:n.2929+41_2929+49delinsCAGGTGAAG