Canonical Allele Identifier: CA2391590915
Gene: CFAP410 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.44333054G= , CM000683.2:g.44333054G= GRCh38
NC_000021.8:g.45752937G= , CM000683.1:g.45752937G= GRCh37
NC_000021.7:g.44577365G= NCBI36
NG_032952.1:g.11349C=

Transcript Alleles

HGVS Amino-acid change
ENST00000339818.9:c.352C= MANE Select ENSP00000344566.4:p.Leu118=
ENST00000325223.7:c.352C= ENSP00000317302.7:p.Leu118=
ENST00000339818.8:c.352C= ENSP00000344566.4:p.Leu118=
ENST00000397956.7:c.352C= ENSP00000381047.3:p.Leu118=
ENST00000462742.1:n.2523C=
ENST00000478674.1:n.411C=
ENST00000496321.5:n.468C=
NM_001271440.1:c.352C= NP_001258369.1:p.Leu118=
NM_001271441.1:c.352C= NP_001258370.1:p.Leu118=
NM_001271442.1:c.229C= NP_001258371.1:p.Leu77=
NM_004928.2:c.352C= NP_004919.1:p.Leu118=
XM_006724051.2:c.427C= XP_006724114.1:p.Leu143=
XM_006724052.2:c.427C= XP_006724115.1:p.Leu143=
XM_006724053.2:c.28C= XP_006724116.1:p.Leu10=
XR_937571.1:n.555C=
XM_006724051.3:c.427C= XP_006724114.1:p.Leu143=
XM_006724053.3:c.28C= XP_006724116.1:p.Leu10=
XM_017028470.1:c.556C= XP_016883959.1:p.Leu186=
XM_017028471.1:c.301C= XP_016883960.1:p.Leu101=
XM_017028472.1:c.28C= XP_016883961.1:p.Leu10=
XR_937571.2:n.562C=
NM_004928.3:c.352C= MANE Select NP_004919.1:p.Leu118=
NM_001271440.2:c.352C= NP_001258369.1:p.Leu118=
NM_001271441.2:c.352C= NP_001258370.1:p.Leu118=