Canonical Allele Identifier: CA410456796

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45753017A>C (hg19) ; chr21:g.44333134A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333134A>C , CM000683.2:g.44333134A>C	GRCh38
NC_000021.8:g.45753017A>C , CM000683.1:g.45753017A>C	GRCh37
NC_000021.7:g.44577445A>C	NCBI36
NG_032952.1:g.11269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.272T>G MANE Select	ENSP00000344566.4:p.Val91Gly
ENST00000325223.7:c.272T>G	ENSP00000317302.7:p.Val91Gly
ENST00000339818.8:c.272T>G	ENSP00000344566.4:p.Val91Gly
ENST00000397956.7:c.272T>G	ENSP00000381047.3:p.Val91Gly
ENST00000462742.1:n.2443T>G
ENST00000478674.1:n.331T>G
ENST00000496321.5:n.388T>G
NM_001271440.1:c.272T>G	NP_001258369.1:p.Val91Gly
NM_001271441.1:c.272T>G	NP_001258370.1:p.Val91Gly
NM_001271442.1:c.149T>G	NP_001258371.1:p.Val50Gly
NM_004928.2:c.272T>G	NP_004919.1:p.Val91Gly
XM_006724051.2:c.347T>G	XP_006724114.1:p.Val116Gly
XM_006724052.2:c.347T>G	XP_006724115.1:p.Val116Gly
XM_006724053.2:c.-53T>G	XP_006724116.1:n.-53T>G
XR_937571.1:n.475T>G
XM_006724051.3:c.347T>G	XP_006724114.1:p.Val116Gly
XM_006724053.3:c.-53T>G	XP_006724116.1:n.-53T>G
XM_017028470.1:c.476T>G	XP_016883959.1:p.Val159Gly
XM_017028471.1:c.221T>G	XP_016883960.1:p.Val74Gly
XM_017028472.1:c.-53T>G	XP_016883961.1:n.-53T>G
XR_937571.2:n.482T>G
NM_004928.3:c.272T>G MANE Select	NP_004919.1:p.Val91Gly
NM_001271440.2:c.272T>G	NP_001258369.1:p.Val91Gly
NM_001271441.2:c.272T>G	NP_001258370.1:p.Val91Gly