Canonical Allele Identifier: CA2221867220
Gene: NOD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50729880A= , CM000678.2:g.50729880A= GRCh38
NC_000016.9:g.50763791A= , CM000678.1:g.50763791A= GRCh37
NC_000016.8:g.49321292A= NCBI36
NG_007508.1:g.37742A= , LRG_177:g.37742A=

Transcript Alleles

HGVS Amino-acid change
ENST00000641284.2:c.*62A= ENSP00000493088.1:n.*62A=
ENST00000646677.2:c.*713A= ENSP00000496533.1:n.*713A=
ENST00000697428.1:n.2426A=
ENST00000641284.1:c.*62A= ENSP00000493088.1:n.*62A=
ENST00000646677.1:c.*713A= ENSP00000496533.1:n.*713A=
ENST00000647318.2:c.2948A= MANE Select ENSP00000495993.1:p.Asn983=
ENST00000300589.6:c.3029A= ENSP00000300589.2:p.Asn1010=
NM_001293557.1:c.2948A= NP_001280486.1:p.Asn983=
NM_022162.2:c.3029A= NP_071445.1:p.Asn1010=
XM_005256084.2:c.2948A= XP_005256141.1:p.Asn983=
XM_006721242.2:c.2864A= XP_006721305.1:p.Asn955=
XM_011523257.1:c.2525A= XP_011521559.1:p.Asn842=
XM_011523258.1:c.2525A= XP_011521560.1:p.Asn842=
XM_011523259.1:c.2363A= XP_011521561.1:p.Asn788=
XM_005256084.4:c.2948A= XP_005256141.1:p.Asn983=
XM_006721242.4:c.2864A= XP_006721305.1:p.Asn955=
XM_011523259.2:c.2363A= XP_011521561.1:p.Asn788=
XM_017023535.1:c.2456A= XP_016879024.1:p.Asn819=
XM_017023536.1:c.2363A= XP_016879025.1:p.Asn788=
XM_017023537.1:c.2363A= XP_016879026.1:p.Asn788=
XM_017023538.1:c.2363A= XP_016879027.1:p.Asn788=
NM_001293557.2:c.2948A= NP_001280486.1:p.Asn983=
NM_001370466.1:c.2948A= MANE Select NP_001357395.1:p.Asn983=
NM_022162.3:c.3029A= NP_071445.1:p.Asn1010=
NR_163434.1:n.3160A=