Canonical Allele Identifier: CA495473116

Gene: NOD2

Linked Data

• gnomAD v4: 16-50722662-C-T
• MyVariant Identifiers: chr16:g.50756573C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722662C>T , CM000678.2:g.50722662C>T	GRCh38
NC_000016.9:g.50756573C>T , CM000678.1:g.50756573C>T	GRCh37
NC_000016.8:g.49314074C>T	NCBI36
NG_007508.1:g.30524C>T , LRG_177:g.30524C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7156C>T	ENSP00000493088.1:n.2382-7156C>T
ENST00000646677.2:c.*439C>T	ENSP00000496533.1:n.*439C>T
ENST00000697425.1:c.501C>T
ENST00000697426.1:c.389C>T
ENST00000697427.1:c.305C>T
ENST00000697428.1:n.2152C>T
ENST00000641284.1:c.2382-7156C>T	ENSP00000493088.1:n.2382-7156C>T
ENST00000646677.1:c.*439C>T	ENSP00000496533.1:n.*439C>T
ENST00000647318.2:c.2674C>T MANE Select	ENSP00000495993.1:p.Leu892=
ENST00000300589.6:c.2755C>T	ENSP00000300589.2:p.Leu919=
ENST00000524712.5:c.249C>T
ENST00000527052.5:c.221C>T
ENST00000529633.5:c.333C>T
ENST00000534057.1:c.389C>T
ENST00000534067.5:c.485C>T
NM_001293557.1:c.2674C>T	NP_001280486.1:p.Leu892=
NM_022162.2:c.2755C>T	NP_071445.1:p.Leu919=
XM_005256084.2:c.2674C>T	XP_005256141.1:p.Leu892=
XM_006721242.2:c.2590C>T	XP_006721305.1:p.Leu864=
XM_011523257.1:c.2251C>T	XP_011521559.1:p.Leu751=
XM_011523258.1:c.2251C>T	XP_011521560.1:p.Leu751=
XM_011523259.1:c.2089C>T	XP_011521561.1:p.Leu697=
XR_429725.2:n.2596C>T
XR_429726.2:n.2512C>T
XR_933387.1:n.2792C>T
XM_005256084.4:c.2674C>T	XP_005256141.1:p.Leu892=
XM_006721242.4:c.2590C>T	XP_006721305.1:p.Leu864=
XM_011523259.2:c.2089C>T	XP_011521561.1:p.Leu697=
XM_017023535.1:c.2182C>T	XP_016879024.1:p.Leu728=
XM_017023536.1:c.2089C>T	XP_016879025.1:p.Leu697=
XM_017023537.1:c.2089C>T	XP_016879026.1:p.Leu697=
XM_017023538.1:c.2089C>T	XP_016879027.1:p.Leu697=
XR_429725.3:n.2549C>T
XR_429726.3:n.2465C>T
XR_933387.2:n.2745C>T
NM_001293557.2:c.2674C>T	NP_001280486.1:p.Leu892=
NM_001370466.1:c.2674C>T MANE Select	NP_001357395.1:p.Leu892=
NM_022162.3:c.2755C>T	NP_071445.1:p.Leu919=
NR_163434.1:n.2886C>T