Canonical Allele Identifier: CA1259751353
Gene: CD207 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831983A= , CM000664.2:g.70831983A= GRCh38
NC_000002.11:g.71059114A= , CM000664.1:g.71059114A= GRCh37
NC_000002.10:g.70912622A= NCBI36
NG_033914.1:g.8841T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000410009.5:c.718-164T= MANE Select ENSP00000386378.3:n.718-164T=
ENST00000410009.4:c.718-164T= ENSP00000386378.3:n.718-164T=
NM_015717.4:c.718-164T= NP_056532.4:n.718-164T=
XM_011532874.1:c.718-164T= XP_011531176.1:n.718-164T=
XM_011532875.1:c.718-164T= XP_011531177.1:n.718-164T=
XM_011532876.1:c.718-164T= XP_011531178.1:n.718-164T=
XM_011532875.2:c.718-164T= XP_011531177.1:n.718-164T=
XM_011532876.2:c.718-164T= XP_011531178.1:n.718-164T=
NM_015717.5:c.718-164T= MANE Select NP_056532.4:n.718-164T=