Canonical Allele Identifier: CA2659494389
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831701-C-CTCACACT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831703_70831709dup , CM000664.2:g.70831703_70831709dup GRCh38
NC_000002.11:g.71058834_71058840dup , CM000664.1:g.71058834_71058840dup GRCh37
NC_000002.10:g.70912342_70912348dup NCBI36
NG_033914.1:g.9116_9122dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.829_835dup MANE Select ENSP00000386378.3:p.Arg279LysfsTer9
ENST00000410009.4:c.829_835dup ENSP00000386378.3:p.Arg279LysfsTer9
NM_015717.4:c.829_835dup NP_056532.4:p.Arg279LysfsTer9
XM_011532874.1:c.829_835dup XP_011531176.1:p.Arg279LysfsTer9
XM_011532875.1:c.829_835dup XP_011531177.1:p.Arg279LysfsTer?
XM_011532876.1:c.829_835dup XP_011531178.1:p.Arg279LysfsTer?
XM_011532875.2:c.829_835dup XP_011531177.1:p.Arg279LysfsTer?
XM_011532876.2:c.829_835dup XP_011531178.1:p.Arg279LysfsTer?
NM_015717.5:c.829_835dup MANE Select NP_056532.4:p.Arg279LysfsTer9
Search 100 bp 5'
Search 100 bp 3'