Canonical Allele Identifier: CA410456321

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45752961T>A (hg19) ; chr21:g.44333078T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333078T>A , CM000683.2:g.44333078T>A	GRCh38
NC_000021.8:g.45752961T>A , CM000683.1:g.45752961T>A	GRCh37
NC_000021.7:g.44577389T>A	NCBI36
NG_032952.1:g.11325A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000339818.9:c.328A>T MANE Select	ENSP00000344566.4:p.Thr110Ser
ENST00000325223.7:c.328A>T	ENSP00000317302.7:p.Thr110Ser
ENST00000339818.8:c.328A>T	ENSP00000344566.4:p.Thr110Ser
ENST00000397956.7:c.328A>T	ENSP00000381047.3:p.Thr110Ser
ENST00000462742.1:n.2499A>T
ENST00000478674.1:n.387A>T
ENST00000496321.5:n.444A>T
NM_001271440.1:c.328A>T	NP_001258369.1:p.Thr110Ser
NM_001271441.1:c.328A>T	NP_001258370.1:p.Thr110Ser
NM_001271442.1:c.205A>T	NP_001258371.1:p.Thr69Ser
NM_004928.2:c.328A>T	NP_004919.1:p.Thr110Ser
XM_006724051.2:c.403A>T	XP_006724114.1:p.Thr135Ser
XM_006724052.2:c.403A>T	XP_006724115.1:p.Thr135Ser
XM_006724053.2:c.4A>T	XP_006724116.1:p.Thr2Ser
XR_937571.1:n.531A>T
XM_006724051.3:c.403A>T	XP_006724114.1:p.Thr135Ser
XM_006724053.3:c.4A>T	XP_006724116.1:p.Thr2Ser
XM_017028470.1:c.532A>T	XP_016883959.1:p.Thr178Ser
XM_017028471.1:c.277A>T	XP_016883960.1:p.Thr93Ser
XM_017028472.1:c.4A>T	XP_016883961.1:p.Thr2Ser
XR_937571.2:n.538A>T
NM_004928.3:c.328A>T MANE Select	NP_004919.1:p.Thr110Ser
NM_001271440.2:c.328A>T	NP_001258369.1:p.Thr110Ser
NM_001271441.2:c.328A>T	NP_001258370.1:p.Thr110Ser