Canonical Allele Identifier: CA2659494341
Gene: CD207 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831647_70831649del , CM000664.2:g.70831647_70831649del GRCh38
NC_000002.11:g.71058778_71058780del , CM000664.1:g.71058778_71058780del GRCh37
NC_000002.10:g.70912286_70912288del NCBI36
NG_033914.1:g.9175_9177del

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.836+52_836+54del MANE Select ENSP00000386378.3:n.836+52_836+54del
ENST00000410009.4:c.836+52_836+54del ENSP00000386378.3:n.836+52_836+54del
NM_015717.4:c.836+52_836+54del NP_056532.4:n.836+52_836+54del
XM_011532874.1:c.836+52_836+54del XP_011531176.1:n.836+52_836+54del
XM_011532875.1:c.836+52_836+54del XP_011531177.1:n.836+52_836+54del
XM_011532876.1:c.836+52_836+54del XP_011531178.1:n.836+52_836+54del
XM_011532875.2:c.836+52_836+54del XP_011531177.1:n.836+52_836+54del
XM_011532876.2:c.836+52_836+54del XP_011531178.1:n.836+52_836+54del
NM_015717.5:c.836+52_836+54del MANE Select NP_056532.4:n.836+52_836+54del