Canonical Allele Identifier: CA2221840729

Gene: NOD2

Linked Data

• dbSNP Id: rs1965098990

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722399_50722404dup , CM000678.2:g.50722399_50722404dup	GRCh38
NC_000016.9:g.50756310_50756315dup , CM000678.1:g.50756310_50756315dup	GRCh37
NC_000016.8:g.49313811_49313816dup	NCBI36
NG_007508.1:g.30261_30266dup , LRG_177:g.30261_30266dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7419_2382-7414dup	ENSP00000493088.1:n.2382-7419_2382-7414dup
ENST00000646677.2:c.*399-223_*399-218dup	ENSP00000496533.1:n.*399-223_*399-218dup
ENST00000697425.1:c.461-223_461-218dup
ENST00000697426.1:c.349-223_349-218dup
ENST00000697427.1:c.265-223_265-218dup
ENST00000697428.1:n.2112-223_2112-218dup
ENST00000641284.1:c.2382-7419_2382-7414dup	ENSP00000493088.1:n.2382-7419_2382-7414dup
ENST00000646677.1:c.*399-223_*399-218dup	ENSP00000496533.1:n.*399-223_*399-218dup
ENST00000647318.2:c.2634-223_2634-218dup MANE Select	ENSP00000495993.1:n.2634-223_2634-218dup
ENST00000300589.6:c.2715-223_2715-218dup	ENSP00000300589.2:n.2715-223_2715-218dup
ENST00000524712.5:c.209-223_209-218dup
ENST00000527052.5:c.181-223_181-218dup
ENST00000529633.5:c.293-223_293-218dup
ENST00000534057.1:c.349-223_349-218dup
ENST00000534067.5:c.445-223_445-218dup
NM_001293557.1:c.2634-223_2634-218dup	NP_001280486.1:n.2634-223_2634-218dup
NM_022162.2:c.2715-223_2715-218dup	NP_071445.1:n.2715-223_2715-218dup
XM_005256084.2:c.2634-223_2634-218dup	XP_005256141.1:n.2634-223_2634-218dup
XM_006721242.2:c.2550-223_2550-218dup	XP_006721305.1:n.2550-223_2550-218dup
XM_011523257.1:c.2211-223_2211-218dup	XP_011521559.1:n.2211-223_2211-218dup
XM_011523258.1:c.2211-223_2211-218dup	XP_011521560.1:n.2211-223_2211-218dup
XM_011523259.1:c.2049-223_2049-218dup	XP_011521561.1:n.2049-223_2049-218dup
XR_429725.2:n.2556-223_2556-218dup
XR_429726.2:n.2472-223_2472-218dup
XR_933387.1:n.2752-223_2752-218dup
XM_005256084.4:c.2634-223_2634-218dup	XP_005256141.1:n.2634-223_2634-218dup
XM_006721242.4:c.2550-223_2550-218dup	XP_006721305.1:n.2550-223_2550-218dup
XM_011523259.2:c.2049-223_2049-218dup	XP_011521561.1:n.2049-223_2049-218dup
XM_017023535.1:c.2142-223_2142-218dup	XP_016879024.1:n.2142-223_2142-218dup
XM_017023536.1:c.2049-223_2049-218dup	XP_016879025.1:n.2049-223_2049-218dup
XM_017023537.1:c.2049-223_2049-218dup	XP_016879026.1:n.2049-223_2049-218dup
XM_017023538.1:c.2049-223_2049-218dup	XP_016879027.1:n.2049-223_2049-218dup
XR_429725.3:n.2509-223_2509-218dup
XR_429726.3:n.2425-223_2425-218dup
XR_933387.2:n.2705-223_2705-218dup
NM_001293557.2:c.2634-223_2634-218dup	NP_001280486.1:n.2634-223_2634-218dup
NM_001370466.1:c.2634-223_2634-218dup MANE Select	NP_001357395.1:n.2634-223_2634-218dup
NM_022162.3:c.2715-223_2715-218dup	NP_071445.1:n.2715-223_2715-218dup
NR_163434.1:n.2846-223_2846-218dup