Canonical Allele Identifier: CA512670989

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45753055A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333172A>G , CM000683.2:g.44333172A>G	GRCh38
NC_000021.8:g.45753055A>G , CM000683.1:g.45753055A>G	GRCh37
NC_000021.7:g.44577483A>G	NCBI36
NG_032952.1:g.11231T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.234T>C MANE Select	ENSP00000344566.4:p.Ala78=
ENST00000325223.7:c.234T>C	ENSP00000317302.7:p.Ala78=
ENST00000339818.8:c.234T>C	ENSP00000344566.4:p.Ala78=
ENST00000397956.7:c.234T>C	ENSP00000381047.3:p.Ala78=
ENST00000462742.1:n.2405T>C
ENST00000478674.1:n.293T>C
ENST00000496321.5:n.350T>C
NM_001271440.1:c.234T>C	NP_001258369.1:p.Ala78=
NM_001271441.1:c.234T>C	NP_001258370.1:p.Ala78=
NM_001271442.1:c.111T>C	NP_001258371.1:p.Ala37=
NM_004928.2:c.234T>C	NP_004919.1:p.Ala78=
XM_006724051.2:c.309T>C	XP_006724114.1:p.Ala103=
XM_006724052.2:c.309T>C	XP_006724115.1:p.Ala103=
XM_006724053.2:c.-91T>C	XP_006724116.1:n.-91T>C
XR_937571.1:n.437T>C
XM_006724051.3:c.309T>C	XP_006724114.1:p.Ala103=
XM_006724053.3:c.-91T>C	XP_006724116.1:n.-91T>C
XM_017028470.1:c.438T>C	XP_016883959.1:p.Ala146=
XM_017028471.1:c.183T>C	XP_016883960.1:p.Ala61=
XM_017028472.1:c.-91T>C	XP_016883961.1:n.-91T>C
XR_937571.2:n.444T>C
NM_004928.3:c.234T>C MANE Select	NP_004919.1:p.Ala78=
NM_001271440.2:c.234T>C	NP_001258369.1:p.Ala78=
NM_001271441.2:c.234T>C	NP_001258370.1:p.Ala78=