Canonical Allele Identifier: CA495473023

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50756566C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722655C>A , CM000678.2:g.50722655C>A	GRCh38
NC_000016.9:g.50756566C>A , CM000678.1:g.50756566C>A	GRCh37
NC_000016.8:g.49314067C>A	NCBI36
NG_007508.1:g.30517C>A , LRG_177:g.30517C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7163C>A	ENSP00000493088.1:n.2382-7163C>A
ENST00000646677.2:c.*432C>A	ENSP00000496533.1:n.*432C>A
ENST00000697425.1:c.494C>A
ENST00000697426.1:c.382C>A
ENST00000697427.1:c.298C>A
ENST00000697428.1:n.2145C>A
ENST00000641284.1:c.2382-7163C>A	ENSP00000493088.1:n.2382-7163C>A
ENST00000646677.1:c.*432C>A	ENSP00000496533.1:n.*432C>A
ENST00000647318.2:c.2667C>A MANE Select	ENSP00000495993.1:p.Ala889=
ENST00000300589.6:c.2748C>A	ENSP00000300589.2:p.Ala916=
ENST00000524712.5:c.242C>A
ENST00000527052.5:c.214C>A
ENST00000529633.5:c.326C>A
ENST00000534057.1:c.382C>A
ENST00000534067.5:c.478C>A
NM_001293557.1:c.2667C>A	NP_001280486.1:p.Ala889=
NM_022162.2:c.2748C>A	NP_071445.1:p.Ala916=
XM_005256084.2:c.2667C>A	XP_005256141.1:p.Ala889=
XM_006721242.2:c.2583C>A	XP_006721305.1:p.Ala861=
XM_011523257.1:c.2244C>A	XP_011521559.1:p.Ala748=
XM_011523258.1:c.2244C>A	XP_011521560.1:p.Ala748=
XM_011523259.1:c.2082C>A	XP_011521561.1:p.Ala694=
XR_429725.2:n.2589C>A
XR_429726.2:n.2505C>A
XR_933387.1:n.2785C>A
XM_005256084.4:c.2667C>A	XP_005256141.1:p.Ala889=
XM_006721242.4:c.2583C>A	XP_006721305.1:p.Ala861=
XM_011523259.2:c.2082C>A	XP_011521561.1:p.Ala694=
XM_017023535.1:c.2175C>A	XP_016879024.1:p.Ala725=
XM_017023536.1:c.2082C>A	XP_016879025.1:p.Ala694=
XM_017023537.1:c.2082C>A	XP_016879026.1:p.Ala694=
XM_017023538.1:c.2082C>A	XP_016879027.1:p.Ala694=
XR_429725.3:n.2542C>A
XR_429726.3:n.2458C>A
XR_933387.2:n.2738C>A
NM_001293557.2:c.2667C>A	NP_001280486.1:p.Ala889=
NM_001370466.1:c.2667C>A MANE Select	NP_001357395.1:p.Ala889=
NM_022162.3:c.2748C>A	NP_071445.1:p.Ala916=
NR_163434.1:n.2879C>A