Canonical Allele Identifier: CA1259751252
Gene: CD207 HGNC NCBI

Linked Data

dbSNP Id: rs1677481071
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831791_70831803del , CM000664.2:g.70831791_70831803del GRCh38
NC_000002.11:g.71058922_71058934del , CM000664.1:g.71058922_71058934del GRCh37
NC_000002.10:g.70912430_70912442del NCBI36
NG_033914.1:g.9023_9035del

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.736_748del MANE Select ENSP00000386378.3:p.Ala246SerfsTer6
ENST00000410009.4:c.736_748del ENSP00000386378.3:p.Ala246SerfsTer6
NM_015717.4:c.736_748del NP_056532.4:p.Ala246SerfsTer6
XM_011532874.1:c.736_748del XP_011531176.1:p.Ala246SerfsTer6
XM_011532875.1:c.736_748del XP_011531177.1:p.Ala246SerfsTer6
XM_011532876.1:c.736_748del XP_011531178.1:p.Ala246SerfsTer6
XM_011532875.2:c.736_748del XP_011531177.1:p.Ala246SerfsTer6
XM_011532876.2:c.736_748del XP_011531178.1:p.Ala246SerfsTer6
NM_015717.5:c.736_748del MANE Select NP_056532.4:p.Ala246SerfsTer6
Search 100 bp 5'
Search 100 bp 3'