Canonical Allele Identifier: CA410448576

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44330314C>G , CM000683.2:g.44330314C>G	GRCh38
NC_000021.8:g.45750197C>G , CM000683.1:g.45750197C>G	GRCh37
NC_000021.7:g.44574625C>G	NCBI36
NG_032952.1:g.14089G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004928.3:c.655G>C MANE Select	NP_004919.1:p.Ala219Pro
ENST00000339818.9:c.655G>C MANE Select	ENSP00000344566.4:p.Ala219Pro
NM_001271440.1:c.652G>C	NP_001258369.1:p.Ala218Pro
NM_001271440.2:c.652G>C	NP_001258369.1:p.Ala218Pro
NM_001271441.1:c.1012G>C	NP_001258370.1:p.Ala338Pro
NM_001271441.2:c.1012G>C	NP_001258370.1:p.Ala338Pro
NM_001271442.1:c.529G>C	NP_001258371.1:p.Ala177Pro
NM_004928.2:c.655G>C	NP_004919.1:p.Ala219Pro
ENST00000325223.7:c.652G>C	ENSP00000317302.7:p.Ala218Pro
ENST00000339818.8:c.655G>C	ENSP00000344566.4:p.Ala219Pro
ENST00000397956.7:c.1012G>C	ENSP00000381047.3:p.Ala338Pro
ENST00000462742.1:n.4109G>C
ENST00000470196.5:n.231G>C
ENST00000496321.5:n.768G>C
XM_006724051.2:c.730G>C	XP_006724114.1:p.Ala244Pro
XM_006724051.3:c.730G>C	XP_006724114.1:p.Ala244Pro
XM_006724052.2:c.727G>C	XP_006724115.1:p.Ala243Pro
XM_006724053.2:c.331G>C	XP_006724116.1:p.Ala111Pro
XM_006724053.3:c.331G>C	XP_006724116.1:p.Ala111Pro
XM_017028470.1:c.856G>C	XP_016883959.1:p.Ala286Pro
XM_017028471.1:c.604G>C	XP_016883960.1:p.Ala202Pro
XM_017028472.1:c.328G>C	XP_016883961.1:p.Ala110Pro
XR_937571.1:n.1215G>C
XR_937571.2:n.1222G>C