Canonical Allele Identifier: CA2750395612
Gene: CD207 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831717del , CM000664.2:g.70831717del GRCh38
NC_000002.11:g.71058848del , CM000664.1:g.71058848del GRCh37
NC_000002.10:g.70912356del NCBI36
NG_033914.1:g.9108del

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.821del MANE Select ENSP00000386378.3:p.Lys274ArgfsTer5
ENST00000410009.4:c.821del ENSP00000386378.3:p.Lys274ArgfsTer5
NM_015717.4:c.821del NP_056532.4:p.Lys274ArgfsTer5
XM_011532874.1:c.821del XP_011531176.1:p.Lys274ArgfsTer5
XM_011532875.1:c.821del XP_011531177.1:p.Lys274ArgfsTer5
XM_011532876.1:c.821del XP_011531178.1:p.Lys274ArgfsTer5
XM_011532875.2:c.821del XP_011531177.1:p.Lys274ArgfsTer5
XM_011532876.2:c.821del XP_011531178.1:p.Lys274ArgfsTer5
NM_015717.5:c.821del MANE Select NP_056532.4:p.Lys274ArgfsTer5
Search 100 bp 5'
Search 100 bp 3'