Canonical Allele Identifier: CA512670950

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45753028C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333145C>G , CM000683.2:g.44333145C>G	GRCh38
NC_000021.8:g.45753028C>G , CM000683.1:g.45753028C>G	GRCh37
NC_000021.7:g.44577456C>G	NCBI36
NG_032952.1:g.11258G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.261G>C MANE Select	ENSP00000344566.4:p.Pro87=
ENST00000325223.7:c.261G>C	ENSP00000317302.7:p.Pro87=
ENST00000339818.8:c.261G>C	ENSP00000344566.4:p.Pro87=
ENST00000397956.7:c.261G>C	ENSP00000381047.3:p.Pro87=
ENST00000462742.1:n.2432G>C
ENST00000478674.1:n.320G>C
ENST00000496321.5:n.377G>C
NM_001271440.1:c.261G>C	NP_001258369.1:p.Pro87=
NM_001271441.1:c.261G>C	NP_001258370.1:p.Pro87=
NM_001271442.1:c.138G>C	NP_001258371.1:p.Pro46=
NM_004928.2:c.261G>C	NP_004919.1:p.Pro87=
XM_006724051.2:c.336G>C	XP_006724114.1:p.Pro112=
XM_006724052.2:c.336G>C	XP_006724115.1:p.Pro112=
XM_006724053.2:c.-64G>C	XP_006724116.1:n.-64G>C
XR_937571.1:n.464G>C
XM_006724051.3:c.336G>C	XP_006724114.1:p.Pro112=
XM_006724053.3:c.-64G>C	XP_006724116.1:n.-64G>C
XM_017028470.1:c.465G>C	XP_016883959.1:p.Pro155=
XM_017028471.1:c.210G>C	XP_016883960.1:p.Pro70=
XM_017028472.1:c.-64G>C	XP_016883961.1:n.-64G>C
XR_937571.2:n.471G>C
NM_004928.3:c.261G>C MANE Select	NP_004919.1:p.Pro87=
NM_001271440.2:c.261G>C	NP_001258369.1:p.Pro87=
NM_001271441.2:c.261G>C	NP_001258370.1:p.Pro87=