Canonical Allele Identifier: CA410456132

Gene: CFAP410

Linked Data

• gnomAD v4: 21-44333034-C-A
• MyVariant Identifiers: chr21:g.45752917C>A (hg19) ; chr21:g.44333034C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333034C>A , CM000683.2:g.44333034C>A	GRCh38
NC_000021.8:g.45752917C>A , CM000683.1:g.45752917C>A	GRCh37
NC_000021.7:g.44577345C>A	NCBI36
NG_032952.1:g.11369G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.372G>T MANE Select	ENSP00000344566.4:p.Gln124His
ENST00000325223.7:c.372G>T	ENSP00000317302.7:p.Gln124His
ENST00000339818.8:c.372G>T	ENSP00000344566.4:p.Gln124His
ENST00000397956.7:c.372G>T	ENSP00000381047.3:p.Gln124His
ENST00000462742.1:n.2543G>T
ENST00000478674.1:n.431G>T
ENST00000496321.5:n.488G>T
NM_001271440.1:c.372G>T	NP_001258369.1:p.Gln124His
NM_001271441.1:c.372G>T	NP_001258370.1:p.Gln124His
NM_001271442.1:c.249G>T	NP_001258371.1:p.Gln83His
NM_004928.2:c.372G>T	NP_004919.1:p.Gln124His
XM_006724051.2:c.447G>T	XP_006724114.1:p.Gln149His
XM_006724052.2:c.447G>T	XP_006724115.1:p.Gln149His
XM_006724053.2:c.48G>T	XP_006724116.1:p.Gln16His
XR_937571.1:n.575G>T
XM_006724051.3:c.447G>T	XP_006724114.1:p.Gln149His
XM_006724053.3:c.48G>T	XP_006724116.1:p.Gln16His
XM_017028470.1:c.576G>T	XP_016883959.1:p.Gln192His
XM_017028471.1:c.321G>T	XP_016883960.1:p.Gln107His
XM_017028472.1:c.48G>T	XP_016883961.1:p.Gln16His
XR_937571.2:n.582G>T
NM_004928.3:c.372G>T MANE Select	NP_004919.1:p.Gln124His
NM_001271440.2:c.372G>T	NP_001258369.1:p.Gln124His
NM_001271441.2:c.372G>T	NP_001258370.1:p.Gln124His