Canonical Allele Identifier: CA410448537
Gene: CFAP410 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44330301A>G , CM000683.2:g.44330301A>G GRCh38
NC_000021.8:g.45750184A>G , CM000683.1:g.45750184A>G GRCh37
NC_000021.7:g.44574612A>G NCBI36
NG_032952.1:g.14102T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000339818.9:c.668T>C MANE Select ENSP00000344566.4:p.Leu223Pro
ENST00000325223.7:c.665T>C ENSP00000317302.7:p.Leu222Pro
ENST00000339818.8:c.668T>C ENSP00000344566.4:p.Leu223Pro
ENST00000397956.7:c.1025T>C ENSP00000381047.3:p.Leu342Pro
ENST00000462742.1:n.4122T>C
ENST00000470196.5:n.244T>C
ENST00000496321.5:n.781T>C
NM_001271440.1:c.665T>C NP_001258369.1:p.Leu222Pro
NM_001271441.1:c.1025T>C NP_001258370.1:p.Leu342Pro
NM_001271442.1:c.542T>C NP_001258371.1:p.Leu181Pro
NM_004928.2:c.668T>C NP_004919.1:p.Leu223Pro
XM_006724051.2:c.743T>C XP_006724114.1:p.Leu248Pro
XM_006724052.2:c.740T>C XP_006724115.1:p.Leu247Pro
XM_006724053.2:c.344T>C XP_006724116.1:p.Leu115Pro
XR_937571.1:n.1228T>C
XM_006724051.3:c.743T>C XP_006724114.1:p.Leu248Pro
XM_006724053.3:c.344T>C XP_006724116.1:p.Leu115Pro
XM_017028470.1:c.869T>C XP_016883959.1:p.Leu290Pro
XM_017028471.1:c.617T>C XP_016883960.1:p.Leu206Pro
XM_017028472.1:c.341T>C XP_016883961.1:p.Leu114Pro
XR_937571.2:n.1235T>C
NM_004928.3:c.668T>C MANE Select NP_004919.1:p.Leu223Pro
NM_001271440.2:c.665T>C NP_001258369.1:p.Leu222Pro
NM_001271441.2:c.1025T>C NP_001258370.1:p.Leu342Pro