Canonical Allele Identifier: CA2576996701

Gene: CD207

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831614_70831618del , CM000664.2:g.70831614_70831618del	GRCh38
NC_000002.11:g.71058745_71058749del , CM000664.1:g.71058745_71058749del	GRCh37
NC_000002.10:g.70912253_70912257del	NCBI36
NG_033914.1:g.9207_9211del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.836+84_836+88del MANE Select	ENSP00000386378.3:n.836+84_836+88del
ENST00000410009.4:c.836+84_836+88del	ENSP00000386378.3:n.836+84_836+88del
NM_015717.4:c.836+84_836+88del	NP_056532.4:n.836+84_836+88del
XM_011532874.1:c.836+84_836+88del	XP_011531176.1:n.836+84_836+88del
XM_011532875.1:c.836+84_836+88del	XP_011531177.1:n.836+84_836+88del
XM_011532876.1:c.836+84_836+88del	XP_011531178.1:n.836+84_836+88del
XM_011532875.2:c.836+84_836+88del	XP_011531177.1:n.836+84_836+88del
XM_011532876.2:c.836+84_836+88del	XP_011531178.1:n.836+84_836+88del
NM_015717.5:c.836+84_836+88del MANE Select	NP_056532.4:n.836+84_836+88del