Canonical Allele Identifier: CA892614340

Gene: CD207

Linked Data

• dbSNP Id: rs1179309133
• MyVariant Identifiers: chr2:g.70831729del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831729del , CM000664.2:g.70831729del	GRCh38
NC_000002.11:g.71058860del , CM000664.1:g.71058860del	GRCh37
NC_000002.10:g.70912368del	NCBI36
NG_033914.1:g.9095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.808del MANE Select	ENSP00000386378.3:p.Thr270ArgfsTer9
ENST00000410009.4:c.808del	ENSP00000386378.3:p.Thr270ArgfsTer9
NM_015717.4:c.808del	NP_056532.4:p.Thr270ArgfsTer9
XM_011532874.1:c.808del	XP_011531176.1:p.Thr270ArgfsTer9
XM_011532875.1:c.808del	XP_011531177.1:p.Thr270ArgfsTer9
XM_011532876.1:c.808del	XP_011531178.1:p.Thr270ArgfsTer9
XM_011532875.2:c.808del	XP_011531177.1:p.Thr270ArgfsTer9
XM_011532876.2:c.808del	XP_011531178.1:p.Thr270ArgfsTer9
NM_015717.5:c.808del MANE Select	NP_056532.4:p.Thr270ArgfsTer9