Canonical Allele Identifier: CA2659495011

Gene: CD207

Linked Data

• gnomAD v4: 2-70831941-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831945_70831946del , CM000664.2:g.70831945_70831946del	GRCh38
NC_000002.11:g.71059076_71059077del , CM000664.1:g.71059076_71059077del	GRCh37
NC_000002.10:g.70912584_70912585del	NCBI36
NG_033914.1:g.8881_8882del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.718-124_718-123del MANE Select	ENSP00000386378.3:n.718-124_718-123del
ENST00000410009.4:c.718-124_718-123del	ENSP00000386378.3:n.718-124_718-123del
NM_015717.4:c.718-124_718-123del	NP_056532.4:n.718-124_718-123del
XM_011532874.1:c.718-124_718-123del	XP_011531176.1:n.718-124_718-123del
XM_011532875.1:c.718-124_718-123del	XP_011531177.1:n.718-124_718-123del
XM_011532876.1:c.718-124_718-123del	XP_011531178.1:n.718-124_718-123del
XM_011532875.2:c.718-124_718-123del	XP_011531177.1:n.718-124_718-123del
XM_011532876.2:c.718-124_718-123del	XP_011531178.1:n.718-124_718-123del
NM_015717.5:c.718-124_718-123del MANE Select	NP_056532.4:n.718-124_718-123del