Canonical Allele Identifier: CA495779139

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50746168G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50712257G>A , CM000678.2:g.50712257G>A	GRCh38
NC_000016.9:g.50746168G>A , CM000678.1:g.50746168G>A	GRCh37
NC_000016.8:g.49303669G>A	NCBI36
NG_007508.1:g.20119G>A , LRG_177:g.20119G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2265G>A	ENSP00000493088.1:p.Leu755=
ENST00000646677.2:c.2265G>A	ENSP00000496533.1:p.Leu755=
ENST00000697425.1:c.64G>A
ENST00000697426.1:c.64G>A
ENST00000697427.1:c.64G>A
ENST00000641284.1:c.2265G>A	ENSP00000493088.1:p.Leu755=
ENST00000646677.1:c.2265G>A	ENSP00000496533.1:p.Leu755=
ENST00000647318.2:c.2265G>A MANE Select	ENSP00000495993.1:p.Leu755=
ENST00000300589.6:c.2346G>A	ENSP00000300589.2:p.Leu782=
ENST00000524712.5:c.64G>A
ENST00000527052.5:c.64G>A
ENST00000529633.5:c.64G>A
ENST00000534057.1:c.64G>A
ENST00000534067.5:c.64G>A
NM_001293557.1:c.2265G>A	NP_001280486.1:p.Leu755=
NM_022162.2:c.2346G>A	NP_071445.1:p.Leu782=
XM_005256084.2:c.2265G>A	XP_005256141.1:p.Leu755=
XM_006721242.2:c.2265G>A	XP_006721305.1:p.Leu755=
XM_006721243.2:c.2265G>A	XP_006721306.1:p.Leu755=
XM_011523257.1:c.1842G>A	XP_011521559.1:p.Leu614=
XM_011523258.1:c.1842G>A	XP_011521560.1:p.Leu614=
XM_011523259.1:c.1680G>A	XP_011521561.1:p.Leu560=
XM_011523260.1:c.2265G>A	XP_011521562.1:p.Leu755=
XM_011523261.1:c.2265G>A	XP_011521563.1:p.Leu755=
XR_429725.2:n.2355G>A
XR_429726.2:n.2355G>A
XR_933387.1:n.2355G>A
XM_005256084.4:c.2265G>A	XP_005256141.1:p.Leu755=
XM_006721242.4:c.2265G>A	XP_006721305.1:p.Leu755=
XM_006721243.4:c.2265G>A	XP_006721306.1:p.Leu755=
XM_011523259.2:c.1680G>A	XP_011521561.1:p.Leu560=
XM_011523260.3:c.2265G>A	XP_011521562.1:p.Leu755=
XM_011523261.2:c.2265G>A	XP_011521563.1:p.Leu755=
XM_017023535.1:c.1773G>A	XP_016879024.1:p.Leu591=
XM_017023536.1:c.1680G>A	XP_016879025.1:p.Leu560=
XM_017023537.1:c.1680G>A	XP_016879026.1:p.Leu560=
XM_017023538.1:c.1680G>A	XP_016879027.1:p.Leu560=
XR_429725.3:n.2308G>A
XR_429726.3:n.2308G>A
XR_933387.2:n.2308G>A
NM_001293557.2:c.2265G>A	NP_001280486.1:p.Leu755=
NM_001370466.1:c.2265G>A MANE Select	NP_001357395.1:p.Leu755=
NM_022162.3:c.2346G>A	NP_071445.1:p.Leu782=
NR_163434.1:n.2330G>A