Canonical Allele Identifier: CA2659494393
Gene: CD207 HGNC NCBI

Linked Data

gnomAD v4: 2-70831704-A-ACG
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831705_70831706insGC , CM000664.2:g.70831705_70831706insGC GRCh38
NC_000002.11:g.71058836_71058837insGC , CM000664.1:g.71058836_71058837insGC GRCh37
NC_000002.10:g.70912344_70912345insGC NCBI36
NG_033914.1:g.9119_9120insCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.832_833insCG MANE Select ENSP00000386378.3:p.Val278AlafsTer2
ENST00000410009.4:c.832_833insCG ENSP00000386378.3:p.Val278AlafsTer2
NM_015717.4:c.832_833insCG NP_056532.4:p.Val278AlafsTer2
XM_011532874.1:c.832_833insCG XP_011531176.1:p.Val278AlafsTer2
XM_011532875.1:c.832_833insCG XP_011531177.1:p.Val278AlafsTer2
XM_011532876.1:c.832_833insCG XP_011531178.1:p.Val278AlafsTer2
XM_011532875.2:c.832_833insCG XP_011531177.1:p.Val278AlafsTer2
XM_011532876.2:c.832_833insCG XP_011531178.1:p.Val278AlafsTer2
NM_015717.5:c.832_833insCG MANE Select NP_056532.4:p.Val278AlafsTer2
Search 100 bp 5'
Search 100 bp 3'