Canonical Allele Identifier: CA2732515422

Gene: NOD2

Linked Data

• dbSNP Id: rs2150833881

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50723104_50723105del , CM000678.2:g.50723104_50723105del	GRCh38
NC_000016.9:g.50757015_50757016del , CM000678.1:g.50757015_50757016del	GRCh37
NC_000016.8:g.49314516_49314517del	NCBI36
NG_007508.1:g.30966_30967del , LRG_177:g.30966_30967del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-6714_2382-6713del	ENSP00000493088.1:n.2382-6714_2382-6713del
ENST00000646677.2:c.*483-197_*483-196del	ENSP00000496533.1:n.*483-197_*483-196del
ENST00000697425.1:c.545-197_545-196del
ENST00000697426.1:c.433-197_433-196del
ENST00000697427.1:c.349-197_349-196del
ENST00000697428.1:n.2196-197_2196-196del
ENST00000641284.1:c.2382-6714_2382-6713del	ENSP00000493088.1:n.2382-6714_2382-6713del
ENST00000646677.1:c.*483-197_*483-196del	ENSP00000496533.1:n.*483-197_*483-196del
ENST00000647318.2:c.2718-197_2718-196del MANE Select	ENSP00000495993.1:n.2718-197_2718-196del
ENST00000300589.6:c.2799-197_2799-196del	ENSP00000300589.2:n.2799-197_2799-196del
ENST00000524712.5:c.293-197_293-196del
ENST00000527052.5:c.265-197_265-196del
ENST00000529633.5:c.377-197_377-196del
ENST00000534057.1:c.433-197_433-196del
ENST00000534067.5:c.529-197_529-196del
NM_001293557.1:c.2718-197_2718-196del	NP_001280486.1:n.2718-197_2718-196del
NM_022162.2:c.2799-197_2799-196del	NP_071445.1:n.2799-197_2799-196del
XM_005256084.2:c.2718-197_2718-196del	XP_005256141.1:n.2718-197_2718-196del
XM_006721242.2:c.2634-197_2634-196del	XP_006721305.1:n.2634-197_2634-196del
XM_011523257.1:c.2295-197_2295-196del	XP_011521559.1:n.2295-197_2295-196del
XM_011523258.1:c.2295-197_2295-196del	XP_011521560.1:n.2295-197_2295-196del
XM_011523259.1:c.2133-197_2133-196del	XP_011521561.1:n.2133-197_2133-196del
XR_429725.2:n.2640-197_2640-196del
XR_429726.2:n.2556-197_2556-196del
XR_933387.1:n.2836-197_2836-196del
XM_005256084.4:c.2718-197_2718-196del	XP_005256141.1:n.2718-197_2718-196del
XM_006721242.4:c.2634-197_2634-196del	XP_006721305.1:n.2634-197_2634-196del
XM_011523259.2:c.2133-197_2133-196del	XP_011521561.1:n.2133-197_2133-196del
XM_017023535.1:c.2226-197_2226-196del	XP_016879024.1:n.2226-197_2226-196del
XM_017023536.1:c.2133-197_2133-196del	XP_016879025.1:n.2133-197_2133-196del
XM_017023537.1:c.2133-197_2133-196del	XP_016879026.1:n.2133-197_2133-196del
XM_017023538.1:c.2133-197_2133-196del	XP_016879027.1:n.2133-197_2133-196del
XR_429725.3:n.2593-197_2593-196del
XR_429726.3:n.2509-197_2509-196del
XR_933387.2:n.2789-197_2789-196del
NM_001293557.2:c.2718-197_2718-196del	NP_001280486.1:n.2718-197_2718-196del
NM_001370466.1:c.2718-197_2718-196del MANE Select	NP_001357395.1:n.2718-197_2718-196del
NM_022162.3:c.2799-197_2799-196del	NP_071445.1:n.2799-197_2799-196del
NR_163434.1:n.2930-197_2930-196del