Canonical Allele Identifier: CA2221842261
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722956_50722959delinsATTT , CM000678.2:g.50722956_50722959delinsATTT GRCh38
NC_000016.9:g.50756867_50756870delinsATTT , CM000678.1:g.50756867_50756870delinsATTT GRCh37
NC_000016.8:g.49314368_49314371delinsATTT NCBI36
NG_007508.1:g.30818_30821delinsATTT , LRG_177:g.30818_30821delinsATTT

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.2382-6862_2382-6859delinsATTT ENSP00000493088.1:n.2382-6862_2382-6859de...
ENST00000646677.2:c.*482+251_*482+254delinsATTT ENSP00000496533.1:n.*482+251_*482+254deli...
ENST00000697425.1:c.544+251_544+254delinsATTT
ENST00000697426.1:c.432+251_432+254delinsATTT
ENST00000697427.1:c.348+251_348+254delinsATTT
ENST00000697428.1:n.2195+251_2195+254delinsATTT
ENST00000641284.1:c.2382-6862_2382-6859delinsATTT ENSP00000493088.1:n.2382-6862_2382-6859de...
ENST00000646677.1:c.*482+251_*482+254delinsATTT ENSP00000496533.1:n.*482+251_*482+254deli...
ENST00000647318.2:c.2717+251_2717+254delinsATTT MANE Select ENSP00000495993.1:n.2717+251_2717+254deli...
ENST00000300589.6:c.2798+251_2798+254delinsATTT ENSP00000300589.2:n.2798+251_2798+254deli...
ENST00000524712.5:c.292+251_292+254delinsATTT
ENST00000527052.5:c.264+251_264+254delinsATTT
ENST00000529633.5:c.376+251_376+254delinsATTT
ENST00000534057.1:c.432+251_432+254delinsATTT
ENST00000534067.5:c.528+251_528+254delinsATTT
NM_001293557.1:c.2717+251_2717+254delinsATTT NP_001280486.1:n.2717+251_2717+254delinsA...
NM_022162.2:c.2798+251_2798+254delinsATTT NP_071445.1:n.2798+251_2798+254delinsATTT...
XM_005256084.2:c.2717+251_2717+254delinsATTT XP_005256141.1:n.2717+251_2717+254delinsA...
XM_006721242.2:c.2633+251_2633+254delinsATTT XP_006721305.1:n.2633+251_2633+254delinsA...
XM_011523257.1:c.2294+251_2294+254delinsATTT XP_011521559.1:n.2294+251_2294+254delinsA...
XM_011523258.1:c.2294+251_2294+254delinsATTT XP_011521560.1:n.2294+251_2294+254delinsA...
XM_011523259.1:c.2132+251_2132+254delinsATTT XP_011521561.1:n.2132+251_2132+254delinsA...
XR_429725.2:n.2639+251_2639+254delinsATTT
XR_429726.2:n.2555+251_2555+254delinsATTT
XR_933387.1:n.2835+251_2835+254delinsATTT
XM_005256084.4:c.2717+251_2717+254delinsATTT XP_005256141.1:n.2717+251_2717+254delinsA...
XM_006721242.4:c.2633+251_2633+254delinsATTT XP_006721305.1:n.2633+251_2633+254delinsA...
XM_011523259.2:c.2132+251_2132+254delinsATTT XP_011521561.1:n.2132+251_2132+254delinsA...
XM_017023535.1:c.2225+251_2225+254delinsATTT XP_016879024.1:n.2225+251_2225+254delinsA...
XM_017023536.1:c.2132+251_2132+254delinsATTT XP_016879025.1:n.2132+251_2132+254delinsA...
XM_017023537.1:c.2132+251_2132+254delinsATTT XP_016879026.1:n.2132+251_2132+254delinsA...
XM_017023538.1:c.2132+251_2132+254delinsATTT XP_016879027.1:n.2132+251_2132+254delinsA...
XR_429725.3:n.2592+251_2592+254delinsATTT
XR_429726.3:n.2508+251_2508+254delinsATTT
XR_933387.2:n.2788+251_2788+254delinsATTT
NM_001293557.2:c.2717+251_2717+254delinsATTT NP_001280486.1:n.2717+251_2717+254delinsA...
NM_001370466.1:c.2717+251_2717+254delinsATTT MANE Select NP_001357395.1:n.2717+251_2717+254delinsA...
NM_022162.3:c.2798+251_2798+254delinsATTT NP_071445.1:n.2798+251_2798+254delinsATTT...
NR_163434.1:n.2929+251_2929+254delinsATTT