Canonical Allele Identifier: CA2576996713
Gene: CD207 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831652del , CM000664.2:g.70831652del GRCh38
NC_000002.11:g.71058783del , CM000664.1:g.71058783del GRCh37
NC_000002.10:g.70912291del NCBI36
NG_033914.1:g.9173del

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+50del MANE Select ENSP00000386378.3:n.836+50del
ENST00000410009.4:c.836+50del ENSP00000386378.3:n.836+50del
NM_015717.4:c.836+50del NP_056532.4:n.836+50del
XM_011532874.1:c.836+50del XP_011531176.1:n.836+50del
XM_011532875.1:c.836+50del XP_011531177.1:n.836+50del
XM_011532876.1:c.836+50del XP_011531178.1:n.836+50del
XM_011532875.2:c.836+50del XP_011531177.1:n.836+50del
XM_011532876.2:c.836+50del XP_011531178.1:n.836+50del
NM_015717.5:c.836+50del MANE Select NP_056532.4:n.836+50del