Canonical Allele Identifier: CA1259751234

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831741_70831742delinsAG , CM000664.2:g.70831741_70831742delinsAG	GRCh38
NC_000002.11:g.71058872_71058873delinsAG , CM000664.1:g.71058872_71058873delinsAG	GRCh37
NC_000002.10:g.70912380_70912381delinsAG	NCBI36
NG_033914.1:g.9082_9083delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.795_796delinsCT MANE Select	ENSP00000386378.3:p.Ser265=
ENST00000410009.4:c.795_796delinsCT	ENSP00000386378.3:p.Ser265=
NM_015717.4:c.795_796delinsCT	NP_056532.4:p.Ser265=
XM_011532874.1:c.795_796delinsCT	XP_011531176.1:p.Ser265=
XM_011532875.1:c.795_796delinsCT	XP_011531177.1:p.Ser265=
XM_011532876.1:c.795_796delinsCT	XP_011531178.1:p.Ser265=
XM_011532875.2:c.795_796delinsCT	XP_011531177.1:p.Ser265=
XM_011532876.2:c.795_796delinsCT	XP_011531178.1:p.Ser265=
NM_015717.5:c.795_796delinsCT MANE Select	NP_056532.4:p.Ser265=