Canonical Allele Identifier: CA2659494381

Gene: CD207

Linked Data

• gnomAD v4: 2-70831688-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831689_70831690dup , CM000664.2:g.70831689_70831690dup	GRCh38
NC_000002.11:g.71058820_71058821dup , CM000664.1:g.71058820_71058821dup	GRCh37
NC_000002.10:g.70912328_70912329dup	NCBI36
NG_033914.1:g.9134_9135dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.836+11_836+12dup MANE Select	ENSP00000386378.3:n.836+11_836+12dup
ENST00000410009.4:c.836+11_836+12dup	ENSP00000386378.3:n.836+11_836+12dup
NM_015717.4:c.836+11_836+12dup	NP_056532.4:n.836+11_836+12dup
XM_011532874.1:c.836+11_836+12dup	XP_011531176.1:n.836+11_836+12dup
XM_011532875.1:c.836+11_836+12dup	XP_011531177.1:n.836+11_836+12dup
XM_011532876.1:c.836+11_836+12dup	XP_011531178.1:n.836+11_836+12dup
XM_011532875.2:c.836+11_836+12dup	XP_011531177.1:n.836+11_836+12dup
XM_011532876.2:c.836+11_836+12dup	XP_011531178.1:n.836+11_836+12dup
NM_015717.5:c.836+11_836+12dup MANE Select	NP_056532.4:n.836+11_836+12dup