Canonical Allele Identifier: CA2659494802

Gene: CD207

Linked Data

• gnomAD v4: 2-70831859-TGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831861_70831863del , CM000664.2:g.70831861_70831863del	GRCh38
NC_000002.11:g.71058992_71058994del , CM000664.1:g.71058992_71058994del	GRCh37
NC_000002.10:g.70912500_70912502del	NCBI36
NG_033914.1:g.8962_8964del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-43_718-41del MANE Select	ENSP00000386378.3:n.718-43_718-41del
ENST00000410009.4:c.718-43_718-41del	ENSP00000386378.3:n.718-43_718-41del
NM_015717.4:c.718-43_718-41del	NP_056532.4:n.718-43_718-41del
XM_011532874.1:c.718-43_718-41del	XP_011531176.1:n.718-43_718-41del
XM_011532875.1:c.718-43_718-41del	XP_011531177.1:n.718-43_718-41del
XM_011532876.1:c.718-43_718-41del	XP_011531178.1:n.718-43_718-41del
XM_011532875.2:c.718-43_718-41del	XP_011531177.1:n.718-43_718-41del
XM_011532876.2:c.718-43_718-41del	XP_011531178.1:n.718-43_718-41del
NM_015717.5:c.718-43_718-41del MANE Select	NP_056532.4:n.718-43_718-41del