Canonical Allele Identifier: CA2391590920

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333059G= , CM000683.2:g.44333059G=	GRCh38
NC_000021.8:g.45752942G= , CM000683.1:g.45752942G=	GRCh37
NC_000021.7:g.44577370G=	NCBI36
NG_032952.1:g.11344C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.347C= MANE Select	ENSP00000344566.4:p.Pro116=
ENST00000325223.7:c.347C=	ENSP00000317302.7:p.Pro116=
ENST00000339818.8:c.347C=	ENSP00000344566.4:p.Pro116=
ENST00000397956.7:c.347C=	ENSP00000381047.3:p.Pro116=
ENST00000462742.1:n.2518C=
ENST00000478674.1:n.406C=
ENST00000496321.5:n.463C=
NM_001271440.1:c.347C=	NP_001258369.1:p.Pro116=
NM_001271441.1:c.347C=	NP_001258370.1:p.Pro116=
NM_001271442.1:c.224C=	NP_001258371.1:p.Pro75=
NM_004928.2:c.347C=	NP_004919.1:p.Pro116=
XM_006724051.2:c.422C=	XP_006724114.1:p.Pro141=
XM_006724052.2:c.422C=	XP_006724115.1:p.Pro141=
XM_006724053.2:c.23C=	XP_006724116.1:p.Pro8=
XR_937571.1:n.550C=
XM_006724051.3:c.422C=	XP_006724114.1:p.Pro141=
XM_006724053.3:c.23C=	XP_006724116.1:p.Pro8=
XM_017028470.1:c.551C=	XP_016883959.1:p.Pro184=
XM_017028471.1:c.296C=	XP_016883960.1:p.Pro99=
XM_017028472.1:c.23C=	XP_016883961.1:p.Pro8=
XR_937571.2:n.557C=
NM_004928.3:c.347C= MANE Select	NP_004919.1:p.Pro116=
NM_001271440.2:c.347C=	NP_001258369.1:p.Pro116=
NM_001271441.2:c.347C=	NP_001258370.1:p.Pro116=