Canonical Allele Identifier: CA2391591054

Gene: CFAP410

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333301A= , CM000683.2:g.44333301A=	GRCh38
NC_000021.8:g.45753184A= , CM000683.1:g.45753184A=	GRCh37
NC_000021.7:g.44577612A=	NCBI36
NG_032952.1:g.11102T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.144-39T= MANE Select	ENSP00000344566.4:n.144-39T=
ENST00000325223.7:c.144-39T=	ENSP00000317302.7:n.144-39T=
ENST00000339818.8:c.144-39T=	ENSP00000344566.4:n.144-39T=
ENST00000397956.7:c.144-39T=	ENSP00000381047.3:n.144-39T=
ENST00000462742.1:n.2315-39T=
ENST00000478674.1:n.164T=
ENST00000496321.5:n.269-48T=
NM_001271440.1:c.144-39T=	NP_001258369.1:n.144-39T=
NM_001271441.1:c.144-39T=	NP_001258370.1:n.144-39T=
NM_001271442.1:c.30-48T=	NP_001258371.1:n.30-48T=
NM_004928.2:c.144-39T=	NP_004919.1:n.144-39T=
XM_006724051.2:c.219-39T=	XP_006724114.1:n.219-39T=
XM_006724052.2:c.219-39T=	XP_006724115.1:n.219-39T=
XM_006724053.2:c.-181-39T=	XP_006724116.1:n.-181-39T=
XR_937571.1:n.347-39T=
XM_006724051.3:c.219-39T=	XP_006724114.1:n.219-39T=
XM_006724053.3:c.-181-39T=	XP_006724116.1:n.-181-39T=
XM_017028470.1:c.348-39T=	XP_016883959.1:n.348-39T=
XM_017028471.1:c.93-39T=	XP_016883960.1:n.93-39T=
XM_017028472.1:c.-181-39T=	XP_016883961.1:n.-181-39T=
XR_937571.2:n.354-39T=
NM_004928.3:c.144-39T= MANE Select	NP_004919.1:n.144-39T=
NM_001271440.2:c.144-39T=	NP_001258369.1:n.144-39T=
NM_001271441.2:c.144-39T=	NP_001258370.1:n.144-39T=