Canonical Allele Identifier: CA2659494336

Gene: CD207

Linked Data

• gnomAD v4: 2-70831640-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831642del , CM000664.2:g.70831642del	GRCh38
NC_000002.11:g.71058773del , CM000664.1:g.71058773del	GRCh37
NC_000002.10:g.70912281del	NCBI36
NG_033914.1:g.9183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.836+60del MANE Select	ENSP00000386378.3:n.836+60del
ENST00000410009.4:c.836+60del	ENSP00000386378.3:n.836+60del
NM_015717.4:c.836+60del	NP_056532.4:n.836+60del
XM_011532874.1:c.836+60del	XP_011531176.1:n.836+60del
XM_011532875.1:c.836+60del	XP_011531177.1:n.836+60del
XM_011532876.1:c.836+60del	XP_011531178.1:n.836+60del
XM_011532875.2:c.836+60del	XP_011531177.1:n.836+60del
XM_011532876.2:c.836+60del	XP_011531178.1:n.836+60del
NM_015717.5:c.836+60del MANE Select	NP_056532.4:n.836+60del