Canonical Allele Identifier: CA2221841888

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722801_50722802delinsAC , CM000678.2:g.50722801_50722802delinsAC	GRCh38
NC_000016.9:g.50756712_50756713delinsAC , CM000678.1:g.50756712_50756713delinsAC	GRCh37
NC_000016.8:g.49314213_49314214delinsAC	NCBI36
NG_007508.1:g.30663_30664delinsAC , LRG_177:g.30663_30664delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7017_2382-7016delinsAC	ENSP00000493088.1:n.2382-7017_2382-7016delinsAC
ENST00000646677.2:c.*482+96_*482+97delinsAC	ENSP00000496533.1:n.*482+96_*482+97delinsAC
ENST00000697425.1:c.544+96_544+97delinsAC
ENST00000697426.1:c.432+96_432+97delinsAC
ENST00000697427.1:c.348+96_348+97delinsAC
ENST00000697428.1:n.2195+96_2195+97delinsAC
ENST00000641284.1:c.2382-7017_2382-7016delinsAC	ENSP00000493088.1:n.2382-7017_2382-7016delinsAC
ENST00000646677.1:c.*482+96_*482+97delinsAC	ENSP00000496533.1:n.*482+96_*482+97delinsAC
ENST00000647318.2:c.2717+96_2717+97delinsAC MANE Select	ENSP00000495993.1:n.2717+96_2717+97delinsAC
ENST00000300589.6:c.2798+96_2798+97delinsAC	ENSP00000300589.2:n.2798+96_2798+97delinsAC
ENST00000524712.5:c.292+96_292+97delinsAC
ENST00000527052.5:c.264+96_264+97delinsAC
ENST00000529633.5:c.376+96_376+97delinsAC
ENST00000534057.1:c.432+96_432+97delinsAC
ENST00000534067.5:c.528+96_528+97delinsAC
NM_001293557.1:c.2717+96_2717+97delinsAC	NP_001280486.1:n.2717+96_2717+97delinsAC
NM_022162.2:c.2798+96_2798+97delinsAC	NP_071445.1:n.2798+96_2798+97delinsAC
XM_005256084.2:c.2717+96_2717+97delinsAC	XP_005256141.1:n.2717+96_2717+97delinsAC
XM_006721242.2:c.2633+96_2633+97delinsAC	XP_006721305.1:n.2633+96_2633+97delinsAC
XM_011523257.1:c.2294+96_2294+97delinsAC	XP_011521559.1:n.2294+96_2294+97delinsAC
XM_011523258.1:c.2294+96_2294+97delinsAC	XP_011521560.1:n.2294+96_2294+97delinsAC
XM_011523259.1:c.2132+96_2132+97delinsAC	XP_011521561.1:n.2132+96_2132+97delinsAC
XR_429725.2:n.2639+96_2639+97delinsAC
XR_429726.2:n.2555+96_2555+97delinsAC
XR_933387.1:n.2835+96_2835+97delinsAC
XM_005256084.4:c.2717+96_2717+97delinsAC	XP_005256141.1:n.2717+96_2717+97delinsAC
XM_006721242.4:c.2633+96_2633+97delinsAC	XP_006721305.1:n.2633+96_2633+97delinsAC
XM_011523259.2:c.2132+96_2132+97delinsAC	XP_011521561.1:n.2132+96_2132+97delinsAC
XM_017023535.1:c.2225+96_2225+97delinsAC	XP_016879024.1:n.2225+96_2225+97delinsAC
XM_017023536.1:c.2132+96_2132+97delinsAC	XP_016879025.1:n.2132+96_2132+97delinsAC
XM_017023537.1:c.2132+96_2132+97delinsAC	XP_016879026.1:n.2132+96_2132+97delinsAC
XM_017023538.1:c.2132+96_2132+97delinsAC	XP_016879027.1:n.2132+96_2132+97delinsAC
XR_429725.3:n.2592+96_2592+97delinsAC
XR_429726.3:n.2508+96_2508+97delinsAC
XR_933387.2:n.2788+96_2788+97delinsAC
NM_001293557.2:c.2717+96_2717+97delinsAC	NP_001280486.1:n.2717+96_2717+97delinsAC
NM_001370466.1:c.2717+96_2717+97delinsAC MANE Select	NP_001357395.1:n.2717+96_2717+97delinsAC
NM_022162.3:c.2798+96_2798+97delinsAC	NP_071445.1:n.2798+96_2798+97delinsAC
NR_163434.1:n.2929+96_2929+97delinsAC