Canonical Allele Identifier: CA1259751344

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831960C= , CM000664.2:g.70831960C=	GRCh38
NC_000002.11:g.71059091C= , CM000664.1:g.71059091C=	GRCh37
NC_000002.10:g.70912599C=	NCBI36
NG_033914.1:g.8864G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-141G= MANE Select	ENSP00000386378.3:n.718-141G=
ENST00000410009.4:c.718-141G=	ENSP00000386378.3:n.718-141G=
NM_015717.4:c.718-141G=	NP_056532.4:n.718-141G=
XM_011532874.1:c.718-141G=	XP_011531176.1:n.718-141G=
XM_011532875.1:c.718-141G=	XP_011531177.1:n.718-141G=
XM_011532876.1:c.718-141G=	XP_011531178.1:n.718-141G=
XM_011532875.2:c.718-141G=	XP_011531177.1:n.718-141G=
XM_011532876.2:c.718-141G=	XP_011531178.1:n.718-141G=
NM_015717.5:c.718-141G= MANE Select	NP_056532.4:n.718-141G=