Canonical Allele Identifier: CA410457564

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45753116A>G (hg19) ; chr21:g.44333233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333233A>G , CM000683.2:g.44333233A>G	GRCh38
NC_000021.8:g.45753116A>G , CM000683.1:g.45753116A>G	GRCh37
NC_000021.7:g.44577544A>G	NCBI36
NG_032952.1:g.11170T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000339818.9:c.173T>C MANE Select	ENSP00000344566.4:p.Val58Ala
ENST00000325223.7:c.173T>C	ENSP00000317302.7:p.Val58Ala
ENST00000339818.8:c.173T>C	ENSP00000344566.4:p.Val58Ala
ENST00000397956.7:c.173T>C	ENSP00000381047.3:p.Val58Ala
ENST00000462742.1:n.2344T>C
ENST00000478674.1:n.232T>C
ENST00000496321.5:n.289T>C
NM_001271440.1:c.173T>C	NP_001258369.1:p.Val58Ala
NM_001271441.1:c.173T>C	NP_001258370.1:p.Val58Ala
NM_001271442.1:c.50T>C	NP_001258371.1:p.Val17Ala
NM_004928.2:c.173T>C	NP_004919.1:p.Val58Ala
XM_006724051.2:c.248T>C	XP_006724114.1:p.Val83Ala
XM_006724052.2:c.248T>C	XP_006724115.1:p.Val83Ala
XM_006724053.2:c.-152T>C	XP_006724116.1:n.-152T>C
XR_937571.1:n.376T>C
XM_006724051.3:c.248T>C	XP_006724114.1:p.Val83Ala
XM_006724053.3:c.-152T>C	XP_006724116.1:n.-152T>C
XM_017028470.1:c.377T>C	XP_016883959.1:p.Val126Ala
XM_017028471.1:c.122T>C	XP_016883960.1:p.Val41Ala
XM_017028472.1:c.-152T>C	XP_016883961.1:n.-152T>C
XR_937571.2:n.383T>C
NM_004928.3:c.173T>C MANE Select	NP_004919.1:p.Val58Ala
NM_001271440.2:c.173T>C	NP_001258369.1:p.Val58Ala
NM_001271441.2:c.173T>C	NP_001258370.1:p.Val58Ala