Canonical Allele Identifier: CA395866992

Gene: NOD2

Linked Data

• gnomAD v4: 16-50699940-A-C
• MyVariant Identifiers: chr16:g.50733851A>C (hg19) ; chr16:g.50699940A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50699940A>C , CM000678.2:g.50699940A>C	GRCh38
NC_000016.9:g.50733851A>C , CM000678.1:g.50733851A>C	GRCh37
NC_000016.8:g.49291352A>C	NCBI36
NG_007508.1:g.7802A>C , LRG_177:g.7802A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.445A>C	ENSP00000493088.1:p.Thr149Pro
ENST00000646677.2:c.445A>C	ENSP00000496533.1:p.Thr149Pro
ENST00000641284.1:c.445A>C	ENSP00000493088.1:p.Thr149Pro
ENST00000646677.1:c.445A>C	ENSP00000496533.1:p.Thr149Pro
ENST00000647318.2:c.445A>C MANE Select	ENSP00000495993.1:p.Thr149Pro
ENST00000300589.6:c.526A>C	ENSP00000300589.2:p.Thr176Pro
ENST00000526417.6:n.513A>C
ENST00000527070.5:c.*1141A>C	ENSP00000435149.1:n.*1141A>C
ENST00000532206.1:n.630A>C
NM_001293557.1:c.445A>C	NP_001280486.1:p.Thr149Pro
NM_022162.2:c.526A>C	NP_071445.1:p.Thr176Pro
XM_005256084.2:c.445A>C	XP_005256141.1:p.Thr149Pro
XM_006721242.2:c.445A>C	XP_006721305.1:p.Thr149Pro
XM_006721243.2:c.445A>C	XP_006721306.1:p.Thr149Pro
XM_011523257.1:c.-52A>C	XP_011521559.1:n.-52A>C
XM_011523258.1:c.-38+6278A>C	XP_011521560.1:n.-38+6278A>C
XM_011523259.1:c.-35A>C	XP_011521561.1:n.-35A>C
XM_011523260.1:c.445A>C	XP_011521562.1:p.Thr149Pro
XM_011523261.1:c.445A>C	XP_011521563.1:p.Thr149Pro
XR_429725.2:n.535A>C
XR_429726.2:n.535A>C
XR_933387.1:n.535A>C
XM_005256084.4:c.445A>C	XP_005256141.1:p.Thr149Pro
XM_006721242.4:c.445A>C	XP_006721305.1:p.Thr149Pro
XM_006721243.4:c.445A>C	XP_006721306.1:p.Thr149Pro
XM_011523259.2:c.-35A>C	XP_011521561.1:n.-35A>C
XM_011523260.3:c.445A>C	XP_011521562.1:p.Thr149Pro
XM_011523261.2:c.445A>C	XP_011521563.1:p.Thr149Pro
XM_017023536.1:c.-127+6278A>C	XP_016879025.1:n.-127+6278A>C
XM_017023537.1:c.-21+6278A>C	XP_016879026.1:n.-21+6278A>C
XR_429725.3:n.488A>C
XR_429726.3:n.488A>C
XR_933387.2:n.488A>C
NM_001293557.2:c.445A>C	NP_001280486.1:p.Thr149Pro
NM_001370466.1:c.445A>C MANE Select	NP_001357395.1:p.Thr149Pro
NM_022162.3:c.526A>C	NP_071445.1:p.Thr176Pro
NR_163434.1:n.510A>C