Canonical Allele Identifier: CA2221842070

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722862_50722863delinsTC , CM000678.2:g.50722862_50722863delinsTC	GRCh38
NC_000016.9:g.50756773_50756774delinsTC , CM000678.1:g.50756773_50756774delinsTC	GRCh37
NC_000016.8:g.49314274_49314275delinsTC	NCBI36
NG_007508.1:g.30724_30725delinsTC , LRG_177:g.30724_30725delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.2382-6956_2382-6955delinsTC	ENSP00000493088.1:n.2382-6956_2382-6955de...
ENST00000646677.2:c.*482+157_*482+158delinsTC	ENSP00000496533.1:n.*482+157_*482+158deli...
ENST00000697425.1:c.544+157_544+158delinsTC
ENST00000697426.1:c.432+157_432+158delinsTC
ENST00000697427.1:c.348+157_348+158delinsTC
ENST00000697428.1:n.2195+157_2195+158delinsTC
ENST00000641284.1:c.2382-6956_2382-6955delinsTC	ENSP00000493088.1:n.2382-6956_2382-6955de...
ENST00000646677.1:c.*482+157_*482+158delinsTC	ENSP00000496533.1:n.*482+157_*482+158deli...
ENST00000647318.2:c.2717+157_2717+158delinsTC MANE Select	ENSP00000495993.1:n.2717+157_2717+158deli...
ENST00000300589.6:c.2798+157_2798+158delinsTC	ENSP00000300589.2:n.2798+157_2798+158deli...
ENST00000524712.5:c.292+157_292+158delinsTC
ENST00000527052.5:c.264+157_264+158delinsTC
ENST00000529633.5:c.376+157_376+158delinsTC
ENST00000534057.1:c.432+157_432+158delinsTC
ENST00000534067.5:c.528+157_528+158delinsTC
NM_001293557.1:c.2717+157_2717+158delinsTC	NP_001280486.1:n.2717+157_2717+158delinsT...
NM_022162.2:c.2798+157_2798+158delinsTC	NP_071445.1:n.2798+157_2798+158delinsTC
XM_005256084.2:c.2717+157_2717+158delinsTC	XP_005256141.1:n.2717+157_2717+158delinsT...
XM_006721242.2:c.2633+157_2633+158delinsTC	XP_006721305.1:n.2633+157_2633+158delinsT...
XM_011523257.1:c.2294+157_2294+158delinsTC	XP_011521559.1:n.2294+157_2294+158delinsT...
XM_011523258.1:c.2294+157_2294+158delinsTC	XP_011521560.1:n.2294+157_2294+158delinsT...
XM_011523259.1:c.2132+157_2132+158delinsTC	XP_011521561.1:n.2132+157_2132+158delinsT...
XR_429725.2:n.2639+157_2639+158delinsTC
XR_429726.2:n.2555+157_2555+158delinsTC
XR_933387.1:n.2835+157_2835+158delinsTC
XM_005256084.4:c.2717+157_2717+158delinsTC	XP_005256141.1:n.2717+157_2717+158delinsT...
XM_006721242.4:c.2633+157_2633+158delinsTC	XP_006721305.1:n.2633+157_2633+158delinsT...
XM_011523259.2:c.2132+157_2132+158delinsTC	XP_011521561.1:n.2132+157_2132+158delinsT...
XM_017023535.1:c.2225+157_2225+158delinsTC	XP_016879024.1:n.2225+157_2225+158delinsT...
XM_017023536.1:c.2132+157_2132+158delinsTC	XP_016879025.1:n.2132+157_2132+158delinsT...
XM_017023537.1:c.2132+157_2132+158delinsTC	XP_016879026.1:n.2132+157_2132+158delinsT...
XM_017023538.1:c.2132+157_2132+158delinsTC	XP_016879027.1:n.2132+157_2132+158delinsT...
XR_429725.3:n.2592+157_2592+158delinsTC
XR_429726.3:n.2508+157_2508+158delinsTC
XR_933387.2:n.2788+157_2788+158delinsTC
NM_001293557.2:c.2717+157_2717+158delinsTC	NP_001280486.1:n.2717+157_2717+158delinsT...
NM_001370466.1:c.2717+157_2717+158delinsTC MANE Select	NP_001357395.1:n.2717+157_2717+158delinsT...
NM_022162.3:c.2798+157_2798+158delinsTC	NP_071445.1:n.2798+157_2798+158delinsTC
NR_163434.1:n.2929+157_2929+158delinsTC