Canonical Allele Identifier: CA2659494391

Gene: CD207

Linked Data

• gnomAD v4: 2-70831702-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70831706_70831707del , CM000664.2:g.70831706_70831707del	GRCh38
NC_000002.11:g.71058837_71058838del , CM000664.1:g.71058837_71058838del	GRCh37
NC_000002.10:g.70912345_70912346del	NCBI36
NG_033914.1:g.9120_9121del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000410009.5:c.833_834del MANE Select	ENSP00000386378.3:p.Val278GlufsTer7
ENST00000410009.4:c.833_834del	ENSP00000386378.3:p.Val278GlufsTer7
NM_015717.4:c.833_834del	NP_056532.4:p.Val278GlufsTer7
XM_011532874.1:c.833_834del	XP_011531176.1:p.Val278GlufsTer7
XM_011532875.1:c.833_834del	XP_011531177.1:p.Val278GlufsTer?
XM_011532876.1:c.833_834del	XP_011531178.1:p.Val278GlufsTer?
XM_011532875.2:c.833_834del	XP_011531177.1:p.Val278GlufsTer?
XM_011532876.2:c.833_834del	XP_011531178.1:p.Val278GlufsTer?
NM_015717.5:c.833_834del MANE Select	NP_056532.4:p.Val278GlufsTer7