Canonical Allele Identifier: CA2321070280
Gene: CD209 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7740242G>C , CM000681.2:g.7740242G>C GRCh38
NC_000019.9:g.7805128G>C , CM000681.1:g.7805128G>C GRCh37
NC_000019.8:g.7711128G>C NCBI36
NG_012167.1:g.12337C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315599.12:c.*2797C>G MANE Select ENSP00000315477.6:n.*2797C>G
ENST00000676543.1:c.70+5276C>G ENSP00000503143.1:n.70+5276C>G
ENST00000678003.1:c.476+1325C>G ENSP00000504497.1:n.476+1325C>G
ENST00000678227.1:n.579+1325C>G
ENST00000678780.1:c.1971+1325C>G ENSP00000503751.1:n.1971+1325C>G
ENST00000315599.11:c.*2797C>G ENSP00000315477.6:n.*2797C>G
NM_001144893.1:c.*2797C>G NP_001138365.1:n.*2797C>G
NM_001144894.1:c.*2797C>G NP_001138366.1:n.*2797C>G
NM_001144895.1:c.*2797C>G NP_001138367.1:n.*2797C>G
NM_001144896.1:c.*2797C>G NP_001138368.1:n.*2797C>G
NM_001144897.1:c.*2797C>G NP_001138369.1:n.*2797C>G
NM_001144899.1:c.*2797C>G NP_001138371.1:n.*2797C>G
NM_021155.3:c.*2797C>G NP_066978.1:n.*2797C>G
NR_026692.1:n.4179C>G
XM_005272472.3:c.*2797C>G XP_005272529.1:n.*2797C>G
XM_005272472.4:c.*2797C>G XP_005272529.1:n.*2797C>G
NM_021155.4:c.*2797C>G MANE Select NP_066978.1:n.*2797C>G
NM_001144893.2:c.*2797C>G NP_001138365.1:n.*2797C>G
NM_001144894.2:c.*2797C>G NP_001138366.1:n.*2797C>G
NM_001144895.2:c.*2797C>G NP_001138367.1:n.*2797C>G
NM_001144896.2:c.*2797C>G NP_001138368.1:n.*2797C>G
NM_001144897.2:c.*2797C>G NP_001138369.1:n.*2797C>G
NM_001144899.2:c.*2797C>G NP_001138371.1:n.*2797C>G
NR_026692.2:n.4135C>G
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