Canonical Allele Identifier: CA395867737

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50744690G>T (hg19) ; chr16:g.50710779G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50710779G>T , CM000678.2:g.50710779G>T	GRCh38
NC_000016.9:g.50744690G>T , CM000678.1:g.50744690G>T	GRCh37
NC_000016.8:g.49302191G>T	NCBI36
NG_007508.1:g.18641G>T , LRG_177:g.18641G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.787G>T	ENSP00000493088.1:p.Asp263Tyr
ENST00000646677.2:c.787G>T	ENSP00000496533.1:p.Asp263Tyr
ENST00000641284.1:c.787G>T	ENSP00000493088.1:p.Asp263Tyr
ENST00000646677.1:c.787G>T	ENSP00000496533.1:p.Asp263Tyr
ENST00000647318.2:c.787G>T MANE Select	ENSP00000495993.1:p.Asp263Tyr
ENST00000300589.6:c.868G>T	ENSP00000300589.2:p.Asp290Tyr
ENST00000526417.6:n.928G>T
ENST00000527070.5:c.*1483G>T	ENSP00000435149.1:n.*1483G>T
ENST00000532206.1:n.866G>T
NM_001293557.1:c.787G>T	NP_001280486.1:p.Asp263Tyr
NM_022162.2:c.868G>T	NP_071445.1:p.Asp290Tyr
XM_005256084.2:c.787G>T	XP_005256141.1:p.Asp263Tyr
XM_006721242.2:c.787G>T	XP_006721305.1:p.Asp263Tyr
XM_006721243.2:c.787G>T	XP_006721306.1:p.Asp263Tyr
XM_011523257.1:c.364G>T	XP_011521559.1:p.Asp122Tyr
XM_011523258.1:c.364G>T	XP_011521560.1:p.Asp122Tyr
XM_011523259.1:c.202G>T	XP_011521561.1:p.Asp68Tyr
XM_011523260.1:c.787G>T	XP_011521562.1:p.Asp263Tyr
XM_011523261.1:c.787G>T	XP_011521563.1:p.Asp263Tyr
XR_429725.2:n.877G>T
XR_429726.2:n.877G>T
XR_933387.1:n.877G>T
XM_005256084.4:c.787G>T	XP_005256141.1:p.Asp263Tyr
XM_006721242.4:c.787G>T	XP_006721305.1:p.Asp263Tyr
XM_006721243.4:c.787G>T	XP_006721306.1:p.Asp263Tyr
XM_011523259.2:c.202G>T	XP_011521561.1:p.Asp68Tyr
XM_011523260.3:c.787G>T	XP_011521562.1:p.Asp263Tyr
XM_011523261.2:c.787G>T	XP_011521563.1:p.Asp263Tyr
XM_017023535.1:c.295G>T	XP_016879024.1:p.Asp99Tyr
XM_017023536.1:c.202G>T	XP_016879025.1:p.Asp68Tyr
XM_017023537.1:c.202G>T	XP_016879026.1:p.Asp68Tyr
XM_017023538.1:c.202G>T	XP_016879027.1:p.Asp68Tyr
XR_429725.3:n.830G>T
XR_429726.3:n.830G>T
XR_933387.2:n.830G>T
NM_001293557.2:c.787G>T	NP_001280486.1:p.Asp263Tyr
NM_001370466.1:c.787G>T MANE Select	NP_001357395.1:p.Asp263Tyr
NM_022162.3:c.868G>T	NP_071445.1:p.Asp290Tyr
NR_163434.1:n.852G>T