Canonical Allele Identifier: CA395875061

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50756550T>A (hg19) ; chr16:g.50722639T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722639T>A , CM000678.2:g.50722639T>A	GRCh38
NC_000016.9:g.50756550T>A , CM000678.1:g.50756550T>A	GRCh37
NC_000016.8:g.49314051T>A	NCBI36
NG_007508.1:g.30501T>A , LRG_177:g.30501T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7179T>A	ENSP00000493088.1:n.2382-7179T>A
ENST00000646677.2:c.*416T>A	ENSP00000496533.1:n.*416T>A
ENST00000697425.1:c.478T>A
ENST00000697426.1:c.366T>A
ENST00000697427.1:c.282T>A
ENST00000697428.1:n.2129T>A
ENST00000641284.1:c.2382-7179T>A	ENSP00000493088.1:n.2382-7179T>A
ENST00000646677.1:c.*416T>A	ENSP00000496533.1:n.*416T>A
ENST00000647318.2:c.2651T>A MANE Select	ENSP00000495993.1:p.Val884Glu
ENST00000300589.6:c.2732T>A	ENSP00000300589.2:p.Val911Glu
ENST00000524712.5:c.226T>A
ENST00000527052.5:c.198T>A
ENST00000529633.5:c.310T>A
ENST00000534057.1:c.366T>A
ENST00000534067.5:c.462T>A
NM_001293557.1:c.2651T>A	NP_001280486.1:p.Val884Glu
NM_022162.2:c.2732T>A	NP_071445.1:p.Val911Glu
XM_005256084.2:c.2651T>A	XP_005256141.1:p.Val884Glu
XM_006721242.2:c.2567T>A	XP_006721305.1:p.Val856Glu
XM_011523257.1:c.2228T>A	XP_011521559.1:p.Val743Glu
XM_011523258.1:c.2228T>A	XP_011521560.1:p.Val743Glu
XM_011523259.1:c.2066T>A	XP_011521561.1:p.Val689Glu
XR_429725.2:n.2573T>A
XR_429726.2:n.2489T>A
XR_933387.1:n.2769T>A
XM_005256084.4:c.2651T>A	XP_005256141.1:p.Val884Glu
XM_006721242.4:c.2567T>A	XP_006721305.1:p.Val856Glu
XM_011523259.2:c.2066T>A	XP_011521561.1:p.Val689Glu
XM_017023535.1:c.2159T>A	XP_016879024.1:p.Val720Glu
XM_017023536.1:c.2066T>A	XP_016879025.1:p.Val689Glu
XM_017023537.1:c.2066T>A	XP_016879026.1:p.Val689Glu
XM_017023538.1:c.2066T>A	XP_016879027.1:p.Val689Glu
XR_429725.3:n.2526T>A
XR_429726.3:n.2442T>A
XR_933387.2:n.2722T>A
NM_001293557.2:c.2651T>A	NP_001280486.1:p.Val884Glu
NM_001370466.1:c.2651T>A MANE Select	NP_001357395.1:p.Val884Glu
NM_022162.3:c.2732T>A	NP_071445.1:p.Val911Glu
NR_163434.1:n.2863T>A