Canonical Allele Identifier: CA2659494388

Gene: CD207

Linked Data

• gnomAD v4: 2-70831696-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831698del , CM000664.2:g.70831698del	GRCh38
NC_000002.11:g.71058829del , CM000664.1:g.71058829del	GRCh37
NC_000002.10:g.70912337del	NCBI36
NG_033914.1:g.9127del

Transcript Alleles

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