Canonical Allele Identifier: CA410456164

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45752924T>A (hg19) ; chr21:g.44333041T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333041T>A , CM000683.2:g.44333041T>A	GRCh38
NC_000021.8:g.45752924T>A , CM000683.1:g.45752924T>A	GRCh37
NC_000021.7:g.44577352T>A	NCBI36
NG_032952.1:g.11362A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.365A>T MANE Select	ENSP00000344566.4:p.Asp122Val
ENST00000325223.7:c.365A>T	ENSP00000317302.7:p.Asp122Val
ENST00000339818.8:c.365A>T	ENSP00000344566.4:p.Asp122Val
ENST00000397956.7:c.365A>T	ENSP00000381047.3:p.Asp122Val
ENST00000462742.1:n.2536A>T
ENST00000478674.1:n.424A>T
ENST00000496321.5:n.481A>T
NM_001271440.1:c.365A>T	NP_001258369.1:p.Asp122Val
NM_001271441.1:c.365A>T	NP_001258370.1:p.Asp122Val
NM_001271442.1:c.242A>T	NP_001258371.1:p.Asp81Val
NM_004928.2:c.365A>T	NP_004919.1:p.Asp122Val
XM_006724051.2:c.440A>T	XP_006724114.1:p.Asp147Val
XM_006724052.2:c.440A>T	XP_006724115.1:p.Asp147Val
XM_006724053.2:c.41A>T	XP_006724116.1:p.Asp14Val
XR_937571.1:n.568A>T
XM_006724051.3:c.440A>T	XP_006724114.1:p.Asp147Val
XM_006724053.3:c.41A>T	XP_006724116.1:p.Asp14Val
XM_017028470.1:c.569A>T	XP_016883959.1:p.Asp190Val
XM_017028471.1:c.314A>T	XP_016883960.1:p.Asp105Val
XM_017028472.1:c.41A>T	XP_016883961.1:p.Asp14Val
XR_937571.2:n.575A>T
NM_004928.3:c.365A>T MANE Select	NP_004919.1:p.Asp122Val
NM_001271440.2:c.365A>T	NP_001258369.1:p.Asp122Val
NM_001271441.2:c.365A>T	NP_001258370.1:p.Asp122Val