Canonical Allele Identifier: CA395866961

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50733837G>C (hg19) ; chr16:g.50699926G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50699926G>C , CM000678.2:g.50699926G>C	GRCh38
NC_000016.9:g.50733837G>C , CM000678.1:g.50733837G>C	GRCh37
NC_000016.8:g.49291338G>C	NCBI36
NG_007508.1:g.7788G>C , LRG_177:g.7788G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.431G>C	ENSP00000493088.1:p.Arg144Thr
ENST00000646677.2:c.431G>C	ENSP00000496533.1:p.Arg144Thr
ENST00000641284.1:c.431G>C	ENSP00000493088.1:p.Arg144Thr
ENST00000646677.1:c.431G>C	ENSP00000496533.1:p.Arg144Thr
ENST00000647318.2:c.431G>C MANE Select	ENSP00000495993.1:p.Arg144Thr
ENST00000300589.6:c.512G>C	ENSP00000300589.2:p.Arg171Thr
ENST00000526417.6:n.499G>C
ENST00000527070.5:c.*1127G>C	ENSP00000435149.1:n.*1127G>C
ENST00000531674.1:c.431G>C	ENSP00000431681.1:p.Arg144Thr
ENST00000532206.1:n.616G>C
NM_001293557.1:c.431G>C	NP_001280486.1:p.Arg144Thr
NM_022162.2:c.512G>C	NP_071445.1:p.Arg171Thr
XM_005256084.2:c.431G>C	XP_005256141.1:p.Arg144Thr
XM_006721242.2:c.431G>C	XP_006721305.1:p.Arg144Thr
XM_006721243.2:c.431G>C	XP_006721306.1:p.Arg144Thr
XM_011523257.1:c.-66G>C	XP_011521559.1:n.-66G>C
XM_011523258.1:c.-38+6264G>C	XP_011521560.1:n.-38+6264G>C
XM_011523259.1:c.-49G>C	XP_011521561.1:n.-49G>C
XM_011523260.1:c.431G>C	XP_011521562.1:p.Arg144Thr
XM_011523261.1:c.431G>C	XP_011521563.1:p.Arg144Thr
XR_429725.2:n.521G>C
XR_429726.2:n.521G>C
XR_933387.1:n.521G>C
XM_005256084.4:c.431G>C	XP_005256141.1:p.Arg144Thr
XM_006721242.4:c.431G>C	XP_006721305.1:p.Arg144Thr
XM_006721243.4:c.431G>C	XP_006721306.1:p.Arg144Thr
XM_011523259.2:c.-49G>C	XP_011521561.1:n.-49G>C
XM_011523260.3:c.431G>C	XP_011521562.1:p.Arg144Thr
XM_011523261.2:c.431G>C	XP_011521563.1:p.Arg144Thr
XM_017023536.1:c.-127+6264G>C	XP_016879025.1:n.-127+6264G>C
XM_017023537.1:c.-21+6264G>C	XP_016879026.1:n.-21+6264G>C
XR_429725.3:n.474G>C
XR_429726.3:n.474G>C
XR_933387.2:n.474G>C
NM_001293557.2:c.431G>C	NP_001280486.1:p.Arg144Thr
NM_001370466.1:c.431G>C MANE Select	NP_001357395.1:p.Arg144Thr
NM_022162.3:c.512G>C	NP_071445.1:p.Arg171Thr
NR_163434.1:n.496G>C