Canonical Allele Identifier: CA495473093

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50756572C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722661C>A , CM000678.2:g.50722661C>A	GRCh38
NC_000016.9:g.50756572C>A , CM000678.1:g.50756572C>A	GRCh37
NC_000016.8:g.49314073C>A	NCBI36
NG_007508.1:g.30523C>A , LRG_177:g.30523C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7157C>A	ENSP00000493088.1:n.2382-7157C>A
ENST00000646677.2:c.*438C>A	ENSP00000496533.1:n.*438C>A
ENST00000697425.1:c.500C>A
ENST00000697426.1:c.388C>A
ENST00000697427.1:c.304C>A
ENST00000697428.1:n.2151C>A
ENST00000641284.1:c.2382-7157C>A	ENSP00000493088.1:n.2382-7157C>A
ENST00000646677.1:c.*438C>A	ENSP00000496533.1:n.*438C>A
ENST00000647318.2:c.2673C>A MANE Select	ENSP00000495993.1:p.Ala891=
ENST00000300589.6:c.2754C>A	ENSP00000300589.2:p.Ala918=
ENST00000524712.5:c.248C>A
ENST00000527052.5:c.220C>A
ENST00000529633.5:c.332C>A
ENST00000534057.1:c.388C>A
ENST00000534067.5:c.484C>A
NM_001293557.1:c.2673C>A	NP_001280486.1:p.Ala891=
NM_022162.2:c.2754C>A	NP_071445.1:p.Ala918=
XM_005256084.2:c.2673C>A	XP_005256141.1:p.Ala891=
XM_006721242.2:c.2589C>A	XP_006721305.1:p.Ala863=
XM_011523257.1:c.2250C>A	XP_011521559.1:p.Ala750=
XM_011523258.1:c.2250C>A	XP_011521560.1:p.Ala750=
XM_011523259.1:c.2088C>A	XP_011521561.1:p.Ala696=
XR_429725.2:n.2595C>A
XR_429726.2:n.2511C>A
XR_933387.1:n.2791C>A
XM_005256084.4:c.2673C>A	XP_005256141.1:p.Ala891=
XM_006721242.4:c.2589C>A	XP_006721305.1:p.Ala863=
XM_011523259.2:c.2088C>A	XP_011521561.1:p.Ala696=
XM_017023535.1:c.2181C>A	XP_016879024.1:p.Ala727=
XM_017023536.1:c.2088C>A	XP_016879025.1:p.Ala696=
XM_017023537.1:c.2088C>A	XP_016879026.1:p.Ala696=
XM_017023538.1:c.2088C>A	XP_016879027.1:p.Ala696=
XR_429725.3:n.2548C>A
XR_429726.3:n.2464C>A
XR_933387.2:n.2744C>A
NM_001293557.2:c.2673C>A	NP_001280486.1:p.Ala891=
NM_001370466.1:c.2673C>A MANE Select	NP_001357395.1:p.Ala891=
NM_022162.3:c.2754C>A	NP_071445.1:p.Ala918=
NR_163434.1:n.2885C>A