Canonical Allele Identifier: CA2659495063
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831964-TGCCCAGA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831972_70831978del , CM000664.2:g.70831972_70831978del GRCh38
NC_000002.11:g.71059103_71059109del , CM000664.1:g.71059103_71059109del GRCh37
NC_000002.10:g.70912611_70912617del NCBI36
NG_033914.1:g.8853_8859del

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-152_718-146del MANE Select ENSP00000386378.3:n.718-152_718-146del
ENST00000410009.4:c.718-152_718-146del ENSP00000386378.3:n.718-152_718-146del
NM_015717.4:c.718-152_718-146del NP_056532.4:n.718-152_718-146del
XM_011532874.1:c.718-152_718-146del XP_011531176.1:n.718-152_718-146del
XM_011532875.1:c.718-152_718-146del XP_011531177.1:n.718-152_718-146del
XM_011532876.1:c.718-152_718-146del XP_011531178.1:n.718-152_718-146del
XM_011532875.2:c.718-152_718-146del XP_011531177.1:n.718-152_718-146del
XM_011532876.2:c.718-152_718-146del XP_011531178.1:n.718-152_718-146del
NM_015717.5:c.718-152_718-146del MANE Select NP_056532.4:n.718-152_718-146del
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