Canonical Allele Identifier: CA2576996711
Gene: CD207 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831649_70831650del , CM000664.2:g.70831649_70831650del GRCh38
NC_000002.11:g.71058780_71058781del , CM000664.1:g.71058780_71058781del GRCh37
NC_000002.10:g.70912288_70912289del NCBI36
NG_033914.1:g.9174_9175del

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+51_836+52del MANE Select ENSP00000386378.3:n.836+51_836+52del
ENST00000410009.4:c.836+51_836+52del ENSP00000386378.3:n.836+51_836+52del
NM_015717.4:c.836+51_836+52del NP_056532.4:n.836+51_836+52del
XM_011532874.1:c.836+51_836+52del XP_011531176.1:n.836+51_836+52del
XM_011532875.1:c.836+51_836+52del XP_011531177.1:n.836+51_836+52del
XM_011532876.1:c.836+51_836+52del XP_011531178.1:n.836+51_836+52del
XM_011532875.2:c.836+51_836+52del XP_011531177.1:n.836+51_836+52del
XM_011532876.2:c.836+51_836+52del XP_011531178.1:n.836+51_836+52del
NM_015717.5:c.836+51_836+52del MANE Select NP_056532.4:n.836+51_836+52del
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