Canonical Allele Identifier: CA2633162698

Gene: NOD2

Linked Data

• gnomAD v4: 16-50699372-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50699372A>T , CM000678.2:g.50699372A>T	GRCh38
NC_000016.9:g.50733283A>T , CM000678.1:g.50733283A>T	GRCh37
NC_000016.8:g.49290784A>T	NCBI36
NG_007508.1:g.7234A>T , LRG_177:g.7234A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.-8-116A>T	ENSP00000493088.1:n.-8-116A>T
ENST00000646677.2:c.-8-116A>T	ENSP00000496533.1:n.-8-116A>T
ENST00000641284.1:c.-8-116A>T	ENSP00000493088.1:n.-8-116A>T
ENST00000646677.1:c.-8-116A>T	ENSP00000496533.1:n.-8-116A>T
ENST00000647318.2:c.-8-116A>T MANE Select	ENSP00000495993.1:n.-8-116A>T
ENST00000300589.6:c.74-116A>T	ENSP00000300589.2:n.74-116A>T
ENST00000526417.6:n.61-116A>T
ENST00000527070.5:c.*689-116A>T	ENSP00000435149.1:n.*689-116A>T
ENST00000531674.1:c.-8-116A>T	ENSP00000431681.1:n.-8-116A>T
ENST00000532206.1:n.178-116A>T
NM_001293557.1:c.-124A>T	NP_001280486.1:n.-124A>T
NM_022162.2:c.74-116A>T	NP_071445.1:n.74-116A>T
XM_005256084.2:c.-8-116A>T	XP_005256141.1:n.-8-116A>T
XM_006721242.2:c.-8-116A>T	XP_006721305.1:n.-8-116A>T
XM_006721243.2:c.-8-116A>T	XP_006721306.1:n.-8-116A>T
XM_011523258.1:c.-38+5710A>T	XP_011521560.1:n.-38+5710A>T
XM_011523260.1:c.-8-116A>T	XP_011521562.1:n.-8-116A>T
XM_011523261.1:c.-8-116A>T	XP_011521563.1:n.-8-116A>T
XR_429725.2:n.83-116A>T
XR_429726.2:n.83-116A>T
XR_933387.1:n.83-116A>T
XM_005256084.4:c.-8-116A>T	XP_005256141.1:n.-8-116A>T
XM_006721242.4:c.-8-116A>T	XP_006721305.1:n.-8-116A>T
XM_006721243.4:c.-8-116A>T	XP_006721306.1:n.-8-116A>T
XM_011523260.3:c.-8-116A>T	XP_011521562.1:n.-8-116A>T
XM_011523261.2:c.-8-116A>T	XP_011521563.1:n.-8-116A>T
XM_017023536.1:c.-127+5710A>T	XP_016879025.1:n.-127+5710A>T
XM_017023537.1:c.-21+5710A>T	XP_016879026.1:n.-21+5710A>T
XR_429725.3:n.36-116A>T
XR_429726.3:n.36-116A>T
XR_933387.2:n.36-116A>T
NM_001370466.1:c.-8-116A>T MANE Select	NP_001357395.1:n.-8-116A>T
NM_022162.3:c.74-116A>T	NP_071445.1:n.74-116A>T
NR_163434.1:n.58-116A>T