Canonical Allele Identifier: CA2321071186
Gene: CD209 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7742141A>C , CM000681.2:g.7742141A>C GRCh38
NC_000019.9:g.7807027A>C , CM000681.1:g.7807027A>C GRCh37
NC_000019.8:g.7713027A>C NCBI36
NG_012167.1:g.10438T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315599.12:c.*898T>G MANE Select ENSP00000315477.6:n.*898T>G
ENST00000676543.1:c.70+3377T>G ENSP00000503143.1:n.70+3377T>G
ENST00000678003.1:c.146-244T>G ENSP00000504497.1:n.146-244T>G
ENST00000678227.1:n.5T>G
ENST00000678780.1:c.1397T>G ENSP00000503751.1:n.1397T>G
ENST00000315599.11:c.*898T>G ENSP00000315477.6:n.*898T>G
NM_001144893.1:c.*898T>G NP_001138365.1:n.*898T>G
NM_001144894.1:c.*898T>G NP_001138366.1:n.*898T>G
NM_001144895.1:c.*898T>G NP_001138367.1:n.*898T>G
NM_001144896.1:c.*898T>G NP_001138368.1:n.*898T>G
NM_001144897.1:c.*898T>G NP_001138369.1:n.*898T>G
NM_001144899.1:c.*898T>G NP_001138371.1:n.*898T>G
NM_021155.3:c.*898T>G NP_066978.1:n.*898T>G
NR_026692.1:n.2280T>G
XM_005272472.3:c.*898T>G XP_005272529.1:n.*898T>G
XM_005272472.4:c.*898T>G XP_005272529.1:n.*898T>G
NM_021155.4:c.*898T>G MANE Select NP_066978.1:n.*898T>G
NM_001144893.2:c.*898T>G NP_001138365.1:n.*898T>G
NM_001144894.2:c.*898T>G NP_001138366.1:n.*898T>G
NM_001144895.2:c.*898T>G NP_001138367.1:n.*898T>G
NM_001144896.2:c.*898T>G NP_001138368.1:n.*898T>G
NM_001144897.2:c.*898T>G NP_001138369.1:n.*898T>G
NM_001144899.2:c.*898T>G NP_001138371.1:n.*898T>G
NR_026692.2:n.2236T>G
Search 100 bp 5'
Search 100 bp 3'