Canonical Allele Identifier: CA395865781
Gene: NOD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50699636C>A , CM000678.2:g.50699636C>A GRCh38
NC_000016.9:g.50733547C>A , CM000678.1:g.50733547C>A GRCh37
NC_000016.8:g.49291048C>A NCBI36
NG_007508.1:g.7498C>A , LRG_177:g.7498C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000641284.2:c.141C>A ENSP00000493088.1:p.Phe47Leu
ENST00000646677.2:c.141C>A ENSP00000496533.1:p.Phe47Leu
ENST00000641284.1:c.141C>A ENSP00000493088.1:p.Phe47Leu
ENST00000646677.1:c.141C>A ENSP00000496533.1:p.Phe47Leu
ENST00000647318.2:c.141C>A MANE Select ENSP00000495993.1:p.Phe47Leu
ENST00000300589.6:c.222C>A ENSP00000300589.2:p.Phe74Leu
ENST00000526417.6:n.209C>A
ENST00000527070.5:c.*837C>A ENSP00000435149.1:n.*837C>A
ENST00000531674.1:c.141C>A ENSP00000431681.1:p.Phe47Leu
ENST00000532206.1:n.326C>A
NM_001293557.1:c.141C>A NP_001280486.1:p.Phe47Leu
NM_022162.2:c.222C>A NP_071445.1:p.Phe74Leu
XM_005256084.2:c.141C>A XP_005256141.1:p.Phe47Leu
XM_006721242.2:c.141C>A XP_006721305.1:p.Phe47Leu
XM_006721243.2:c.141C>A XP_006721306.1:p.Phe47Leu
XM_011523258.1:c.-38+5974C>A XP_011521560.1:n.-38+5974C>A
XM_011523259.1:c.-339C>A XP_011521561.1:n.-339C>A
XM_011523260.1:c.141C>A XP_011521562.1:p.Phe47Leu
XM_011523261.1:c.141C>A XP_011521563.1:p.Phe47Leu
XR_429725.2:n.231C>A
XR_429726.2:n.231C>A
XR_933387.1:n.231C>A
XM_005256084.4:c.141C>A XP_005256141.1:p.Phe47Leu
XM_006721242.4:c.141C>A XP_006721305.1:p.Phe47Leu
XM_006721243.4:c.141C>A XP_006721306.1:p.Phe47Leu
XM_011523259.2:c.-339C>A XP_011521561.1:n.-339C>A
XM_011523260.3:c.141C>A XP_011521562.1:p.Phe47Leu
XM_011523261.2:c.141C>A XP_011521563.1:p.Phe47Leu
XM_017023536.1:c.-127+5974C>A XP_016879025.1:n.-127+5974C>A
XM_017023537.1:c.-21+5974C>A XP_016879026.1:n.-21+5974C>A
XR_429725.3:n.184C>A
XR_429726.3:n.184C>A
XR_933387.2:n.184C>A
NM_001293557.2:c.141C>A NP_001280486.1:p.Phe47Leu
NM_001370466.1:c.141C>A MANE Select NP_001357395.1:p.Phe47Leu
NM_022162.3:c.222C>A NP_071445.1:p.Phe74Leu
NR_163434.1:n.206C>A