Canonical Allele Identifier: CA395870956

Gene: NOD2

Linked Data

• gnomAD v4: 16-50712024-G-C
• MyVariant Identifiers: chr16:g.50745935G>C (hg19) ; chr16:g.50712024G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50712024G>C , CM000678.2:g.50712024G>C	GRCh38
NC_000016.9:g.50745935G>C , CM000678.1:g.50745935G>C	GRCh37
NC_000016.8:g.49303436G>C	NCBI36
NG_007508.1:g.19886G>C , LRG_177:g.19886G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.2032G>C	ENSP00000493088.1:p.Ala678Pro
ENST00000646677.2:c.2032G>C	ENSP00000496533.1:p.Ala678Pro
ENST00000641284.1:c.2032G>C	ENSP00000493088.1:p.Ala678Pro
ENST00000646677.1:c.2032G>C	ENSP00000496533.1:p.Ala678Pro
ENST00000647318.2:c.2032G>C MANE Select	ENSP00000495993.1:p.Ala678Pro
ENST00000300589.6:c.2113G>C	ENSP00000300589.2:p.Ala705Pro
NM_001293557.1:c.2032G>C	NP_001280486.1:p.Ala678Pro
NM_022162.2:c.2113G>C	NP_071445.1:p.Ala705Pro
XM_005256084.2:c.2032G>C	XP_005256141.1:p.Ala678Pro
XM_006721242.2:c.2032G>C	XP_006721305.1:p.Ala678Pro
XM_006721243.2:c.2032G>C	XP_006721306.1:p.Ala678Pro
XM_011523257.1:c.1609G>C	XP_011521559.1:p.Ala537Pro
XM_011523258.1:c.1609G>C	XP_011521560.1:p.Ala537Pro
XM_011523259.1:c.1447G>C	XP_011521561.1:p.Ala483Pro
XM_011523260.1:c.2032G>C	XP_011521562.1:p.Ala678Pro
XM_011523261.1:c.2032G>C	XP_011521563.1:p.Ala678Pro
XR_429725.2:n.2122G>C
XR_429726.2:n.2122G>C
XR_933387.1:n.2122G>C
XM_005256084.4:c.2032G>C	XP_005256141.1:p.Ala678Pro
XM_006721242.4:c.2032G>C	XP_006721305.1:p.Ala678Pro
XM_006721243.4:c.2032G>C	XP_006721306.1:p.Ala678Pro
XM_011523259.2:c.1447G>C	XP_011521561.1:p.Ala483Pro
XM_011523260.3:c.2032G>C	XP_011521562.1:p.Ala678Pro
XM_011523261.2:c.2032G>C	XP_011521563.1:p.Ala678Pro
XM_017023535.1:c.1540G>C	XP_016879024.1:p.Ala514Pro
XM_017023536.1:c.1447G>C	XP_016879025.1:p.Ala483Pro
XM_017023537.1:c.1447G>C	XP_016879026.1:p.Ala483Pro
XM_017023538.1:c.1447G>C	XP_016879027.1:p.Ala483Pro
XR_429725.3:n.2075G>C
XR_429726.3:n.2075G>C
XR_933387.2:n.2075G>C
NM_001293557.2:c.2032G>C	NP_001280486.1:p.Ala678Pro
NM_001370466.1:c.2032G>C MANE Select	NP_001357395.1:p.Ala678Pro
NM_022162.3:c.2113G>C	NP_071445.1:p.Ala705Pro
NR_163434.1:n.2097G>C