Canonical Allele Identifier: CA1259751235

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831743G= , CM000664.2:g.70831743G=	GRCh38
NC_000002.11:g.71058874G= , CM000664.1:g.71058874G=	GRCh37
NC_000002.10:g.70912382G=	NCBI36
NG_033914.1:g.9081C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.794C= MANE Select	ENSP00000386378.3:p.Ser265=
ENST00000410009.4:c.794C=	ENSP00000386378.3:p.Ser265=
NM_015717.4:c.794C=	NP_056532.4:p.Ser265=
XM_011532874.1:c.794C=	XP_011531176.1:p.Ser265=
XM_011532875.1:c.794C=	XP_011531177.1:p.Ser265=
XM_011532876.1:c.794C=	XP_011531178.1:p.Ser265=
XM_011532875.2:c.794C=	XP_011531177.1:p.Ser265=
XM_011532876.2:c.794C=	XP_011531178.1:p.Ser265=
NM_015717.5:c.794C= MANE Select	NP_056532.4:p.Ser265=