Canonical Allele Identifier: CA395871945

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50746174T>G (hg19) ; chr16:g.50712263T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50712263T>G , CM000678.2:g.50712263T>G	GRCh38
NC_000016.9:g.50746174T>G , CM000678.1:g.50746174T>G	GRCh37
NC_000016.8:g.49303675T>G	NCBI36
NG_007508.1:g.20125T>G , LRG_177:g.20125T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2271T>G	ENSP00000493088.1:p.Phe757Leu
ENST00000646677.2:c.2271T>G	ENSP00000496533.1:p.Phe757Leu
ENST00000697425.1:c.70T>G
ENST00000697426.1:c.70T>G
ENST00000697427.1:c.70T>G
ENST00000641284.1:c.2271T>G	ENSP00000493088.1:p.Phe757Leu
ENST00000646677.1:c.2271T>G	ENSP00000496533.1:p.Phe757Leu
ENST00000647318.2:c.2271T>G MANE Select	ENSP00000495993.1:p.Phe757Leu
ENST00000300589.6:c.2352T>G	ENSP00000300589.2:p.Phe784Leu
ENST00000524712.5:c.70T>G
ENST00000527052.5:c.70T>G
ENST00000529633.5:c.70T>G
ENST00000534057.1:c.70T>G
ENST00000534067.5:c.70T>G
NM_001293557.1:c.2271T>G	NP_001280486.1:p.Phe757Leu
NM_022162.2:c.2352T>G	NP_071445.1:p.Phe784Leu
XM_005256084.2:c.2271T>G	XP_005256141.1:p.Phe757Leu
XM_006721242.2:c.2271T>G	XP_006721305.1:p.Phe757Leu
XM_006721243.2:c.2271T>G	XP_006721306.1:p.Phe757Leu
XM_011523257.1:c.1848T>G	XP_011521559.1:p.Phe616Leu
XM_011523258.1:c.1848T>G	XP_011521560.1:p.Phe616Leu
XM_011523259.1:c.1686T>G	XP_011521561.1:p.Phe562Leu
XM_011523260.1:c.2271T>G	XP_011521562.1:p.Phe757Leu
XM_011523261.1:c.2271T>G	XP_011521563.1:p.Phe757Leu
XR_429725.2:n.2361T>G
XR_429726.2:n.2361T>G
XR_933387.1:n.2361T>G
XM_005256084.4:c.2271T>G	XP_005256141.1:p.Phe757Leu
XM_006721242.4:c.2271T>G	XP_006721305.1:p.Phe757Leu
XM_006721243.4:c.2271T>G	XP_006721306.1:p.Phe757Leu
XM_011523259.2:c.1686T>G	XP_011521561.1:p.Phe562Leu
XM_011523260.3:c.2271T>G	XP_011521562.1:p.Phe757Leu
XM_011523261.2:c.2271T>G	XP_011521563.1:p.Phe757Leu
XM_017023535.1:c.1779T>G	XP_016879024.1:p.Phe593Leu
XM_017023536.1:c.1686T>G	XP_016879025.1:p.Phe562Leu
XM_017023537.1:c.1686T>G	XP_016879026.1:p.Phe562Leu
XM_017023538.1:c.1686T>G	XP_016879027.1:p.Phe562Leu
XR_429725.3:n.2314T>G
XR_429726.3:n.2314T>G
XR_933387.2:n.2314T>G
NM_001293557.2:c.2271T>G	NP_001280486.1:p.Phe757Leu
NM_001370466.1:c.2271T>G MANE Select	NP_001357395.1:p.Phe757Leu
NM_022162.3:c.2352T>G	NP_071445.1:p.Phe784Leu
NR_163434.1:n.2336T>G