Canonical Allele Identifier: CA395876674

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50763741C>G (hg19) ; chr16:g.50729830C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50729830C>G , CM000678.2:g.50729830C>G	GRCh38
NC_000016.9:g.50763741C>G , CM000678.1:g.50763741C>G	GRCh37
NC_000016.8:g.49321242C>G	NCBI36
NG_007508.1:g.37692C>G , LRG_177:g.37692C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.*12C>G	ENSP00000493088.1:n.*12C>G
ENST00000646677.2:c.*663C>G	ENSP00000496533.1:n.*663C>G
ENST00000697428.1:n.2376C>G
ENST00000641284.1:c.*12C>G	ENSP00000493088.1:n.*12C>G
ENST00000646677.1:c.*663C>G	ENSP00000496533.1:n.*663C>G
ENST00000647318.2:c.2898C>G MANE Select	ENSP00000495993.1:p.Asn966Lys
ENST00000300589.6:c.2979C>G	ENSP00000300589.2:p.Asn993Lys
NM_001293557.1:c.2898C>G	NP_001280486.1:p.Asn966Lys
NM_022162.2:c.2979C>G	NP_071445.1:p.Asn993Lys
XM_005256084.2:c.2898C>G	XP_005256141.1:p.Asn966Lys
XM_006721242.2:c.2814C>G	XP_006721305.1:p.Asn938Lys
XM_011523257.1:c.2475C>G	XP_011521559.1:p.Asn825Lys
XM_011523258.1:c.2475C>G	XP_011521560.1:p.Asn825Lys
XM_011523259.1:c.2313C>G	XP_011521561.1:p.Asn771Lys
XM_005256084.4:c.2898C>G	XP_005256141.1:p.Asn966Lys
XM_006721242.4:c.2814C>G	XP_006721305.1:p.Asn938Lys
XM_011523259.2:c.2313C>G	XP_011521561.1:p.Asn771Lys
XM_017023535.1:c.2406C>G	XP_016879024.1:p.Asn802Lys
XM_017023536.1:c.2313C>G	XP_016879025.1:p.Asn771Lys
XM_017023537.1:c.2313C>G	XP_016879026.1:p.Asn771Lys
XM_017023538.1:c.2313C>G	XP_016879027.1:p.Asn771Lys
NM_001293557.2:c.2898C>G	NP_001280486.1:p.Asn966Lys
NM_001370466.1:c.2898C>G MANE Select	NP_001357395.1:p.Asn966Lys
NM_022162.3:c.2979C>G	NP_071445.1:p.Asn993Lys
NR_163434.1:n.3110C>G