Canonical Allele Identifier: CA1259751388

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70832070C= , CM000664.2:g.70832070C=	GRCh38
NC_000002.11:g.71059201C= , CM000664.1:g.71059201C=	GRCh37
NC_000002.10:g.70912709C=	NCBI36
NG_033914.1:g.8754G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-251G= MANE Select	ENSP00000386378.3:n.718-251G=
ENST00000410009.4:c.718-251G=	ENSP00000386378.3:n.718-251G=
NM_015717.4:c.718-251G=	NP_056532.4:n.718-251G=
XM_011532874.1:c.718-251G=	XP_011531176.1:n.718-251G=
XM_011532875.1:c.718-251G=	XP_011531177.1:n.718-251G=
XM_011532876.1:c.718-251G=	XP_011531178.1:n.718-251G=
XM_011532875.2:c.718-251G=	XP_011531177.1:n.718-251G=
XM_011532876.2:c.718-251G=	XP_011531178.1:n.718-251G=
NM_015717.5:c.718-251G= MANE Select	NP_056532.4:n.718-251G=