Canonical Allele Identifier: CA721359378

Gene: NOD2

Linked Data

• dbSNP Id: rs1312500841
• MyVariant Identifiers: chr16:g.50756253_50756258del (hg19) ; chr16:g.50722342_50722347del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722344_50722349del , CM000678.2:g.50722344_50722349del	GRCh38
NC_000016.9:g.50756255_50756260del , CM000678.1:g.50756255_50756260del	GRCh37
NC_000016.8:g.49313756_49313761del	NCBI36
NG_007508.1:g.30206_30211del , LRG_177:g.30206_30211del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7474_2382-7469del	ENSP00000493088.1:n.2382-7474_2382-7469del
ENST00000646677.2:c.*399-278_*399-273del	ENSP00000496533.1:n.*399-278_*399-273del
ENST00000697425.1:c.461-278_461-273del
ENST00000697426.1:c.349-278_349-273del
ENST00000697427.1:c.265-278_265-273del
ENST00000697428.1:n.2112-278_2112-273del
ENST00000641284.1:c.2382-7474_2382-7469del	ENSP00000493088.1:n.2382-7474_2382-7469del
ENST00000646677.1:c.*399-278_*399-273del	ENSP00000496533.1:n.*399-278_*399-273del
ENST00000647318.2:c.2634-278_2634-273del MANE Select	ENSP00000495993.1:n.2634-278_2634-273del
ENST00000300589.6:c.2715-278_2715-273del	ENSP00000300589.2:n.2715-278_2715-273del
ENST00000524712.5:c.209-278_209-273del
ENST00000527052.5:c.181-278_181-273del
ENST00000529633.5:c.293-278_293-273del
ENST00000534057.1:c.349-278_349-273del
ENST00000534067.5:c.445-278_445-273del
NM_001293557.1:c.2634-278_2634-273del	NP_001280486.1:n.2634-278_2634-273del
NM_022162.2:c.2715-278_2715-273del	NP_071445.1:n.2715-278_2715-273del
XM_005256084.2:c.2634-278_2634-273del	XP_005256141.1:n.2634-278_2634-273del
XM_006721242.2:c.2550-278_2550-273del	XP_006721305.1:n.2550-278_2550-273del
XM_011523257.1:c.2211-278_2211-273del	XP_011521559.1:n.2211-278_2211-273del
XM_011523258.1:c.2211-278_2211-273del	XP_011521560.1:n.2211-278_2211-273del
XM_011523259.1:c.2049-278_2049-273del	XP_011521561.1:n.2049-278_2049-273del
XR_429725.2:n.2556-278_2556-273del
XR_429726.2:n.2472-278_2472-273del
XR_933387.1:n.2752-278_2752-273del
XM_005256084.4:c.2634-278_2634-273del	XP_005256141.1:n.2634-278_2634-273del
XM_006721242.4:c.2550-278_2550-273del	XP_006721305.1:n.2550-278_2550-273del
XM_011523259.2:c.2049-278_2049-273del	XP_011521561.1:n.2049-278_2049-273del
XM_017023535.1:c.2142-278_2142-273del	XP_016879024.1:n.2142-278_2142-273del
XM_017023536.1:c.2049-278_2049-273del	XP_016879025.1:n.2049-278_2049-273del
XM_017023537.1:c.2049-278_2049-273del	XP_016879026.1:n.2049-278_2049-273del
XM_017023538.1:c.2049-278_2049-273del	XP_016879027.1:n.2049-278_2049-273del
XR_429725.3:n.2509-278_2509-273del
XR_429726.3:n.2425-278_2425-273del
XR_933387.2:n.2705-278_2705-273del
NM_001293557.2:c.2634-278_2634-273del	NP_001280486.1:n.2634-278_2634-273del
NM_001370466.1:c.2634-278_2634-273del MANE Select	NP_001357395.1:n.2634-278_2634-273del
NM_022162.3:c.2715-278_2715-273del	NP_071445.1:n.2715-278_2715-273del
NR_163434.1:n.2846-278_2846-273del