Canonical Allele Identifier: CA410456171

Gene: CFAP410

Linked Data

• ClinVar Variation Id: 812236
• ClinVar RCV Id: RCV002267748 ; RCV001860522
• dbSNP Id: rs1602079250
• MyVariant Identifiers: chr21:g.45752925C>T (hg19) ; chr21:g.44333042C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333042C>T , CM000683.2:g.44333042C>T	GRCh38
NC_000021.8:g.45752925C>T , CM000683.1:g.45752925C>T	GRCh37
NC_000021.7:g.44577353C>T	NCBI36
NG_032952.1:g.11361G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.364G>A MANE Select	ENSP00000344566.4:p.Asp122Asn
ENST00000325223.7:c.364G>A	ENSP00000317302.7:p.Asp122Asn
ENST00000339818.8:c.364G>A	ENSP00000344566.4:p.Asp122Asn
ENST00000397956.7:c.364G>A	ENSP00000381047.3:p.Asp122Asn
ENST00000462742.1:n.2535G>A
ENST00000478674.1:n.423G>A
ENST00000496321.5:n.480G>A
NM_001271440.1:c.364G>A	NP_001258369.1:p.Asp122Asn
NM_001271441.1:c.364G>A	NP_001258370.1:p.Asp122Asn
NM_001271442.1:c.241G>A	NP_001258371.1:p.Asp81Asn
NM_004928.2:c.364G>A	NP_004919.1:p.Asp122Asn
XM_006724051.2:c.439G>A	XP_006724114.1:p.Asp147Asn
XM_006724052.2:c.439G>A	XP_006724115.1:p.Asp147Asn
XM_006724053.2:c.40G>A	XP_006724116.1:p.Asp14Asn
XR_937571.1:n.567G>A
XM_006724051.3:c.439G>A	XP_006724114.1:p.Asp147Asn
XM_006724053.3:c.40G>A	XP_006724116.1:p.Asp14Asn
XM_017028470.1:c.568G>A	XP_016883959.1:p.Asp190Asn
XM_017028471.1:c.313G>A	XP_016883960.1:p.Asp105Asn
XM_017028472.1:c.40G>A	XP_016883961.1:p.Asp14Asn
XR_937571.2:n.574G>A
NM_004928.3:c.364G>A MANE Select	NP_004919.1:p.Asp122Asn
NM_001271440.2:c.364G>A	NP_001258369.1:p.Asp122Asn
NM_001271441.2:c.364G>A	NP_001258370.1:p.Asp122Asn