Canonical Allele Identifier: CA410448626

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44330327C>G , CM000683.2:g.44330327C>G	GRCh38
NC_000021.8:g.45750210C>G , CM000683.1:g.45750210C>G	GRCh37
NC_000021.7:g.44574638C>G	NCBI36
NG_032952.1:g.14076G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004928.3:c.643-1G>C MANE Select	NP_004919.1:n.643-1G>C
ENST00000339818.9:c.643-1G>C MANE Select	ENSP00000344566.4:n.643-1G>C
NM_001271440.1:c.640-1G>C	NP_001258369.1:n.640-1G>C
NM_001271440.2:c.640-1G>C	NP_001258369.1:n.640-1G>C
NM_001271441.1:c.1000-1G>C	NP_001258370.1:n.1000-1G>C
NM_001271441.2:c.1000-1G>C	NP_001258370.1:n.1000-1G>C
NM_001271442.1:c.517-1G>C	NP_001258371.1:n.517-1G>C
NM_004928.2:c.643-1G>C	NP_004919.1:n.643-1G>C
ENST00000325223.7:c.640-1G>C	ENSP00000317302.7:n.640-1G>C
ENST00000339818.8:c.643-1G>C	ENSP00000344566.4:n.643-1G>C
ENST00000397956.7:c.1000-1G>C	ENSP00000381047.3:n.1000-1G>C
ENST00000462742.1:n.4097-1G>C
ENST00000470196.5:n.219-1G>C
ENST00000496321.5:n.756-1G>C
XM_006724051.2:c.718-1G>C	XP_006724114.1:n.718-1G>C
XM_006724051.3:c.718-1G>C	XP_006724114.1:n.718-1G>C
XM_006724052.2:c.715-1G>C	XP_006724115.1:n.715-1G>C
XM_006724053.2:c.319-1G>C	XP_006724116.1:n.319-1G>C
XM_006724053.3:c.319-1G>C	XP_006724116.1:n.319-1G>C
XM_017028470.1:c.844-1G>C	XP_016883959.1:n.844-1G>C
XM_017028471.1:c.592-1G>C	XP_016883960.1:n.592-1G>C
XM_017028472.1:c.316-1G>C	XP_016883961.1:n.316-1G>C
XR_937571.1:n.1203-1G>C
XR_937571.2:n.1210-1G>C