Canonical Allele Identifier: CA2654807806

Gene: CFAP410

Linked Data

• gnomAD v4: 21-44333022-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333022C>A , CM000683.2:g.44333022C>A	GRCh38
NC_000021.8:g.45752905C>A , CM000683.1:g.45752905C>A	GRCh37
NC_000021.7:g.44577333C>A	NCBI36
NG_032952.1:g.11381G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.373+11G>T MANE Select	ENSP00000344566.4:n.373+11G>T
ENST00000325223.7:c.373+11G>T	ENSP00000317302.7:n.373+11G>T
ENST00000339818.8:c.373+11G>T	ENSP00000344566.4:n.373+11G>T
ENST00000397956.7:c.373+11G>T	ENSP00000381047.3:n.373+11G>T
ENST00000462742.1:n.2544+11G>T
ENST00000478674.1:n.432+11G>T
ENST00000496321.5:n.489+11G>T
NM_001271440.1:c.373+11G>T	NP_001258369.1:n.373+11G>T
NM_001271441.1:c.373+11G>T	NP_001258370.1:n.373+11G>T
NM_001271442.1:c.250+11G>T	NP_001258371.1:n.250+11G>T
NM_004928.2:c.373+11G>T	NP_004919.1:n.373+11G>T
XM_006724051.2:c.448+11G>T	XP_006724114.1:n.448+11G>T
XM_006724052.2:c.448+11G>T	XP_006724115.1:n.448+11G>T
XM_006724053.2:c.49+11G>T	XP_006724116.1:n.49+11G>T
XR_937571.1:n.576+11G>T
XM_006724051.3:c.448+11G>T	XP_006724114.1:n.448+11G>T
XM_006724053.3:c.49+11G>T	XP_006724116.1:n.49+11G>T
XM_017028470.1:c.577+11G>T	XP_016883959.1:n.577+11G>T
XM_017028471.1:c.322+11G>T	XP_016883960.1:n.322+11G>T
XM_017028472.1:c.49+11G>T	XP_016883961.1:n.49+11G>T
XR_937571.2:n.583+11G>T
NM_004928.3:c.373+11G>T MANE Select	NP_004919.1:n.373+11G>T
NM_001271440.2:c.373+11G>T	NP_001258369.1:n.373+11G>T
NM_001271441.2:c.373+11G>T	NP_001258370.1:n.373+11G>T