Canonical Allele Identifier: CA495479274

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50763783T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50729872T>A , CM000678.2:g.50729872T>A	GRCh38
NC_000016.9:g.50763783T>A , CM000678.1:g.50763783T>A	GRCh37
NC_000016.8:g.49321284T>A	NCBI36
NG_007508.1:g.37734T>A , LRG_177:g.37734T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000641284.2:c.*54T>A	ENSP00000493088.1:n.*54T>A
ENST00000646677.2:c.*705T>A	ENSP00000496533.1:n.*705T>A
ENST00000697428.1:n.2418T>A
ENST00000641284.1:c.*54T>A	ENSP00000493088.1:n.*54T>A
ENST00000646677.1:c.*705T>A	ENSP00000496533.1:n.*705T>A
ENST00000647318.2:c.2940T>A MANE Select	ENSP00000495993.1:p.Leu980=
ENST00000300589.6:c.3021T>A	ENSP00000300589.2:p.Leu1007=
NM_001293557.1:c.2940T>A	NP_001280486.1:p.Leu980=
NM_022162.2:c.3021T>A	NP_071445.1:p.Leu1007=
XM_005256084.2:c.2940T>A	XP_005256141.1:p.Leu980=
XM_006721242.2:c.2856T>A	XP_006721305.1:p.Leu952=
XM_011523257.1:c.2517T>A	XP_011521559.1:p.Leu839=
XM_011523258.1:c.2517T>A	XP_011521560.1:p.Leu839=
XM_011523259.1:c.2355T>A	XP_011521561.1:p.Leu785=
XM_005256084.4:c.2940T>A	XP_005256141.1:p.Leu980=
XM_006721242.4:c.2856T>A	XP_006721305.1:p.Leu952=
XM_011523259.2:c.2355T>A	XP_011521561.1:p.Leu785=
XM_017023535.1:c.2448T>A	XP_016879024.1:p.Leu816=
XM_017023536.1:c.2355T>A	XP_016879025.1:p.Leu785=
XM_017023537.1:c.2355T>A	XP_016879026.1:p.Leu785=
XM_017023538.1:c.2355T>A	XP_016879027.1:p.Leu785=
NM_001293557.2:c.2940T>A	NP_001280486.1:p.Leu980=
NM_001370466.1:c.2940T>A MANE Select	NP_001357395.1:p.Leu980=
NM_022162.3:c.3021T>A	NP_071445.1:p.Leu1007=
NR_163434.1:n.3152T>A