Canonical Allele Identifier: CA1259751347

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831971A= , CM000664.2:g.70831971A=	GRCh38
NC_000002.11:g.71059102A= , CM000664.1:g.71059102A=	GRCh37
NC_000002.10:g.70912610A=	NCBI36
NG_033914.1:g.8853T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-152T= MANE Select	ENSP00000386378.3:n.718-152T=
ENST00000410009.4:c.718-152T=	ENSP00000386378.3:n.718-152T=
NM_015717.4:c.718-152T=	NP_056532.4:n.718-152T=
XM_011532874.1:c.718-152T=	XP_011531176.1:n.718-152T=
XM_011532875.1:c.718-152T=	XP_011531177.1:n.718-152T=
XM_011532876.1:c.718-152T=	XP_011531178.1:n.718-152T=
XM_011532875.2:c.718-152T=	XP_011531177.1:n.718-152T=
XM_011532876.2:c.718-152T=	XP_011531178.1:n.718-152T=
NM_015717.5:c.718-152T= MANE Select	NP_056532.4:n.718-152T=