Canonical Allele Identifier: CA2659495066
Gene: CD207 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831968del , CM000664.2:g.70831968del GRCh38
NC_000002.11:g.71059099del , CM000664.1:g.71059099del GRCh37
NC_000002.10:g.70912607del NCBI36
NG_033914.1:g.8858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-147del MANE Select ENSP00000386378.3:n.718-147del
ENST00000410009.4:c.718-147del ENSP00000386378.3:n.718-147del
NM_015717.4:c.718-147del NP_056532.4:n.718-147del
XM_011532874.1:c.718-147del XP_011531176.1:n.718-147del
XM_011532875.1:c.718-147del XP_011531177.1:n.718-147del
XM_011532876.1:c.718-147del XP_011531178.1:n.718-147del
XM_011532875.2:c.718-147del XP_011531177.1:n.718-147del
XM_011532876.2:c.718-147del XP_011531178.1:n.718-147del
NM_015717.5:c.718-147del MANE Select NP_056532.4:n.718-147del