Canonical Allele Identifier: CA1259751238
Gene: CD207 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70831747A= , CM000664.2:g.70831747A= GRCh38
NC_000002.11:g.71058878A= , CM000664.1:g.71058878A= GRCh37
NC_000002.10:g.70912386A= NCBI36
NG_033914.1:g.9077T=

Transcript Alleles

HGVS Amino-acid change
ENST00000410009.5:c.790T= MANE Select ENSP00000386378.3:p.Trp264=
ENST00000410009.4:c.790T= ENSP00000386378.3:p.Trp264=
NM_015717.4:c.790T= NP_056532.4:p.Trp264=
XM_011532874.1:c.790T= XP_011531176.1:p.Trp264=
XM_011532875.1:c.790T= XP_011531177.1:p.Trp264=
XM_011532876.1:c.790T= XP_011531178.1:p.Trp264=
XM_011532875.2:c.790T= XP_011531177.1:p.Trp264=
XM_011532876.2:c.790T= XP_011531178.1:p.Trp264=
NM_015717.5:c.790T= MANE Select NP_056532.4:p.Trp264=