Canonical Allele Identifier: CA395869520

Gene: NOD2

Linked Data

• COSMIC: COSM971302
• MyVariant Identifiers: chr16:g.50745557G>T (hg19) ; chr16:g.50711646G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50711646G>T , CM000678.2:g.50711646G>T	GRCh38
NC_000016.9:g.50745557G>T , CM000678.1:g.50745557G>T	GRCh37
NC_000016.8:g.49303058G>T	NCBI36
NG_007508.1:g.19508G>T , LRG_177:g.19508G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.1654G>T	ENSP00000493088.1:p.Asp552Tyr
ENST00000646677.2:c.1654G>T	ENSP00000496533.1:p.Asp552Tyr
ENST00000641284.1:c.1654G>T	ENSP00000493088.1:p.Asp552Tyr
ENST00000646677.1:c.1654G>T	ENSP00000496533.1:p.Asp552Tyr
ENST00000647318.2:c.1654G>T MANE Select	ENSP00000495993.1:p.Asp552Tyr
ENST00000300589.6:c.1735G>T	ENSP00000300589.2:p.Asp579Tyr
NM_001293557.1:c.1654G>T	NP_001280486.1:p.Asp552Tyr
NM_022162.2:c.1735G>T	NP_071445.1:p.Asp579Tyr
XM_005256084.2:c.1654G>T	XP_005256141.1:p.Asp552Tyr
XM_006721242.2:c.1654G>T	XP_006721305.1:p.Asp552Tyr
XM_006721243.2:c.1654G>T	XP_006721306.1:p.Asp552Tyr
XM_011523257.1:c.1231G>T	XP_011521559.1:p.Asp411Tyr
XM_011523258.1:c.1231G>T	XP_011521560.1:p.Asp411Tyr
XM_011523259.1:c.1069G>T	XP_011521561.1:p.Asp357Tyr
XM_011523260.1:c.1654G>T	XP_011521562.1:p.Asp552Tyr
XM_011523261.1:c.1654G>T	XP_011521563.1:p.Asp552Tyr
XR_429725.2:n.1744G>T
XR_429726.2:n.1744G>T
XR_933387.1:n.1744G>T
XM_005256084.4:c.1654G>T	XP_005256141.1:p.Asp552Tyr
XM_006721242.4:c.1654G>T	XP_006721305.1:p.Asp552Tyr
XM_006721243.4:c.1654G>T	XP_006721306.1:p.Asp552Tyr
XM_011523259.2:c.1069G>T	XP_011521561.1:p.Asp357Tyr
XM_011523260.3:c.1654G>T	XP_011521562.1:p.Asp552Tyr
XM_011523261.2:c.1654G>T	XP_011521563.1:p.Asp552Tyr
XM_017023535.1:c.1162G>T	XP_016879024.1:p.Asp388Tyr
XM_017023536.1:c.1069G>T	XP_016879025.1:p.Asp357Tyr
XM_017023537.1:c.1069G>T	XP_016879026.1:p.Asp357Tyr
XM_017023538.1:c.1069G>T	XP_016879027.1:p.Asp357Tyr
XR_429725.3:n.1697G>T
XR_429726.3:n.1697G>T
XR_933387.2:n.1697G>T
NM_001293557.2:c.1654G>T	NP_001280486.1:p.Asp552Tyr
NM_001370466.1:c.1654G>T MANE Select	NP_001357395.1:p.Asp552Tyr
NM_022162.3:c.1735G>T	NP_071445.1:p.Asp579Tyr
NR_163434.1:n.1719G>T