Canonical Allele Identifier: CA395876943

Gene: NOD2

Linked Data

• gnomAD v4: 16-50729895-A-C
• MyVariant Identifiers: chr16:g.50763806A>C (hg19) ; chr16:g.50729895A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50729895A>C , CM000678.2:g.50729895A>C	GRCh38
NC_000016.9:g.50763806A>C , CM000678.1:g.50763806A>C	GRCh37
NC_000016.8:g.49321307A>C	NCBI36
NG_007508.1:g.37757A>C , LRG_177:g.37757A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.*77A>C	ENSP00000493088.1:n.*77A>C
ENST00000646677.2:c.*728A>C	ENSP00000496533.1:n.*728A>C
ENST00000697428.1:n.2441A>C
ENST00000641284.1:c.*77A>C	ENSP00000493088.1:n.*77A>C
ENST00000646677.1:c.*728A>C	ENSP00000496533.1:n.*728A>C
ENST00000647318.2:c.2963A>C MANE Select	ENSP00000495993.1:p.Glu988Ala
ENST00000300589.6:c.3044A>C	ENSP00000300589.2:p.Glu1015Ala
NM_001293557.1:c.2963A>C	NP_001280486.1:p.Glu988Ala
NM_022162.2:c.3044A>C	NP_071445.1:p.Glu1015Ala
XM_005256084.2:c.2963A>C	XP_005256141.1:p.Glu988Ala
XM_006721242.2:c.2879A>C	XP_006721305.1:p.Glu960Ala
XM_011523257.1:c.2540A>C	XP_011521559.1:p.Glu847Ala
XM_011523258.1:c.2540A>C	XP_011521560.1:p.Glu847Ala
XM_011523259.1:c.2378A>C	XP_011521561.1:p.Glu793Ala
XM_005256084.4:c.2963A>C	XP_005256141.1:p.Glu988Ala
XM_006721242.4:c.2879A>C	XP_006721305.1:p.Glu960Ala
XM_011523259.2:c.2378A>C	XP_011521561.1:p.Glu793Ala
XM_017023535.1:c.2471A>C	XP_016879024.1:p.Glu824Ala
XM_017023536.1:c.2378A>C	XP_016879025.1:p.Glu793Ala
XM_017023537.1:c.2378A>C	XP_016879026.1:p.Glu793Ala
XM_017023538.1:c.2378A>C	XP_016879027.1:p.Glu793Ala
NM_001293557.2:c.2963A>C	NP_001280486.1:p.Glu988Ala
NM_001370466.1:c.2963A>C MANE Select	NP_001357395.1:p.Glu988Ala
NM_022162.3:c.3044A>C	NP_071445.1:p.Glu1015Ala
NR_163434.1:n.3175A>C