Canonical Allele Identifier: CA2221868146
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50732126G= , CM000678.2:g.50732126G= GRCh38
NC_000016.9:g.50766037G= , CM000678.1:g.50766037G= GRCh37
NC_000016.8:g.49323538G= NCBI36
NG_007508.1:g.39988G= , LRG_177:g.39988G=

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.*463G= ENSP00000493088.1:n.*463G=
ENST00000646677.2:c.*1114G= ENSP00000496533.1:n.*1114G=
ENST00000697428.1:n.2827G=
ENST00000641284.1:c.*463G= ENSP00000493088.1:n.*463G=
ENST00000646677.1:c.*1114G= ENSP00000496533.1:n.*1114G=
ENST00000647318.2:c.*307G= MANE Select ENSP00000495993.1:n.*307G=
ENST00000300589.6:c.*307G= ENSP00000300589.2:n.*307G=
NM_001293557.1:c.*307G= NP_001280486.1:n.*307G=
NM_022162.2:c.*307G= NP_071445.1:n.*307G=
XM_005256084.2:c.*307G= XP_005256141.1:n.*307G=
XM_006721242.2:c.*307G= XP_006721305.1:n.*307G=
XM_011523257.1:c.*307G= XP_011521559.1:n.*307G=
XM_011523258.1:c.*307G= XP_011521560.1:n.*307G=
XM_011523259.1:c.*307G= XP_011521561.1:n.*307G=
XM_005256084.4:c.*307G= XP_005256141.1:n.*307G=
XM_006721242.4:c.*307G= XP_006721305.1:n.*307G=
XM_011523259.2:c.*307G= XP_011521561.1:n.*307G=
XM_017023535.1:c.*307G= XP_016879024.1:n.*307G=
XM_017023536.1:c.*307G= XP_016879025.1:n.*307G=
XM_017023537.1:c.*307G= XP_016879026.1:n.*307G=
XM_017023538.1:c.*307G= XP_016879027.1:n.*307G=
NM_001293557.2:c.*307G= NP_001280486.1:n.*307G=
NM_001370466.1:c.*307G= MANE Select NP_001357395.1:n.*307G=
NM_022162.3:c.*307G= NP_071445.1:n.*307G=
NR_163434.1:n.3561G=