Canonical Allele Identifier: CA2576996724
Gene: CD207 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831832del , CM000664.2:g.70831832del GRCh38
NC_000002.11:g.71058963del , CM000664.1:g.71058963del GRCh37
NC_000002.10:g.70912471del NCBI36
NG_033914.1:g.8992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-13del MANE Select ENSP00000386378.3:n.718-13del
ENST00000410009.4:c.718-13del ENSP00000386378.3:n.718-13del
NM_015717.4:c.718-13del NP_056532.4:n.718-13del
XM_011532874.1:c.718-13del XP_011531176.1:n.718-13del
XM_011532875.1:c.718-13del XP_011531177.1:n.718-13del
XM_011532876.1:c.718-13del XP_011531178.1:n.718-13del
XM_011532875.2:c.718-13del XP_011531177.1:n.718-13del
XM_011532876.2:c.718-13del XP_011531178.1:n.718-13del
NM_015717.5:c.718-13del MANE Select NP_056532.4:n.718-13del