Canonical Allele Identifier: CA2659494546
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831793-T-TG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831793_70831794insG , CM000664.2:g.70831793_70831794insG GRCh38
NC_000002.11:g.71058924_71058925insG , CM000664.1:g.71058924_71058925insG GRCh37
NC_000002.10:g.70912432_70912433insG NCBI36
NG_033914.1:g.9030_9031insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.743_744insC MANE Select ENSP00000386378.3:p.Leu249ThrfsTer9
ENST00000410009.4:c.743_744insC ENSP00000386378.3:p.Leu249ThrfsTer9
NM_015717.4:c.743_744insC NP_056532.4:p.Leu249ThrfsTer9
XM_011532874.1:c.743_744insC XP_011531176.1:p.Leu249ThrfsTer9
XM_011532875.1:c.743_744insC XP_011531177.1:p.Leu249ThrfsTer9
XM_011532876.1:c.743_744insC XP_011531178.1:p.Leu249ThrfsTer9
XM_011532875.2:c.743_744insC XP_011531177.1:p.Leu249ThrfsTer9
XM_011532876.2:c.743_744insC XP_011531178.1:p.Leu249ThrfsTer9
NM_015717.5:c.743_744insC MANE Select NP_056532.4:p.Leu249ThrfsTer9
Search 100 bp 5'
Search 100 bp 3'