Canonical Allele Identifier: CA395868057

Gene: NOD2

Linked Data

• gnomAD v4: 16-50710928-G-A
• MyVariant Identifiers: chr16:g.50744839G>A (hg19) ; chr16:g.50710928G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50710928G>A , CM000678.2:g.50710928G>A	GRCh38
NC_000016.9:g.50744839G>A , CM000678.1:g.50744839G>A	GRCh37
NC_000016.8:g.49302340G>A	NCBI36
NG_007508.1:g.18790G>A , LRG_177:g.18790G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.936G>A	ENSP00000493088.1:p.Met312Ile
ENST00000646677.2:c.936G>A	ENSP00000496533.1:p.Met312Ile
ENST00000641284.1:c.936G>A	ENSP00000493088.1:p.Met312Ile
ENST00000646677.1:c.936G>A	ENSP00000496533.1:p.Met312Ile
ENST00000647318.2:c.936G>A MANE Select	ENSP00000495993.1:p.Met312Ile
ENST00000300589.6:c.1017G>A	ENSP00000300589.2:p.Met339Ile
ENST00000526417.6:n.1077G>A
NM_001293557.1:c.936G>A	NP_001280486.1:p.Met312Ile
NM_022162.2:c.1017G>A	NP_071445.1:p.Met339Ile
XM_005256084.2:c.936G>A	XP_005256141.1:p.Met312Ile
XM_006721242.2:c.936G>A	XP_006721305.1:p.Met312Ile
XM_006721243.2:c.936G>A	XP_006721306.1:p.Met312Ile
XM_011523257.1:c.513G>A	XP_011521559.1:p.Met171Ile
XM_011523258.1:c.513G>A	XP_011521560.1:p.Met171Ile
XM_011523259.1:c.351G>A	XP_011521561.1:p.Met117Ile
XM_011523260.1:c.936G>A	XP_011521562.1:p.Met312Ile
XM_011523261.1:c.936G>A	XP_011521563.1:p.Met312Ile
XR_429725.2:n.1026G>A
XR_429726.2:n.1026G>A
XR_933387.1:n.1026G>A
XM_005256084.4:c.936G>A	XP_005256141.1:p.Met312Ile
XM_006721242.4:c.936G>A	XP_006721305.1:p.Met312Ile
XM_006721243.4:c.936G>A	XP_006721306.1:p.Met312Ile
XM_011523259.2:c.351G>A	XP_011521561.1:p.Met117Ile
XM_011523260.3:c.936G>A	XP_011521562.1:p.Met312Ile
XM_011523261.2:c.936G>A	XP_011521563.1:p.Met312Ile
XM_017023535.1:c.444G>A	XP_016879024.1:p.Met148Ile
XM_017023536.1:c.351G>A	XP_016879025.1:p.Met117Ile
XM_017023537.1:c.351G>A	XP_016879026.1:p.Met117Ile
XM_017023538.1:c.351G>A	XP_016879027.1:p.Met117Ile
XR_429725.3:n.979G>A
XR_429726.3:n.979G>A
XR_933387.2:n.979G>A
NM_001293557.2:c.936G>A	NP_001280486.1:p.Met312Ile
NM_001370466.1:c.936G>A MANE Select	NP_001357395.1:p.Met312Ile
NM_022162.3:c.1017G>A	NP_071445.1:p.Met339Ile
NR_163434.1:n.1001G>A