Canonical Allele Identifier: CA512670913

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45753007C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333124C>A , CM000683.2:g.44333124C>A	GRCh38
NC_000021.8:g.45753007C>A , CM000683.1:g.45753007C>A	GRCh37
NC_000021.7:g.44577435C>A	NCBI36
NG_032952.1:g.11279G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.282G>T MANE Select	ENSP00000344566.4:p.Leu94=
ENST00000325223.7:c.282G>T	ENSP00000317302.7:p.Leu94=
ENST00000339818.8:c.282G>T	ENSP00000344566.4:p.Leu94=
ENST00000397956.7:c.282G>T	ENSP00000381047.3:p.Leu94=
ENST00000462742.1:n.2453G>T
ENST00000478674.1:n.341G>T
ENST00000496321.5:n.398G>T
NM_001271440.1:c.282G>T	NP_001258369.1:p.Leu94=
NM_001271441.1:c.282G>T	NP_001258370.1:p.Leu94=
NM_001271442.1:c.159G>T	NP_001258371.1:p.Leu53=
NM_004928.2:c.282G>T	NP_004919.1:p.Leu94=
XM_006724051.2:c.357G>T	XP_006724114.1:p.Leu119=
XM_006724052.2:c.357G>T	XP_006724115.1:p.Leu119=
XM_006724053.2:c.-43G>T	XP_006724116.1:n.-43G>T
XR_937571.1:n.485G>T
XM_006724051.3:c.357G>T	XP_006724114.1:p.Leu119=
XM_006724053.3:c.-43G>T	XP_006724116.1:n.-43G>T
XM_017028470.1:c.486G>T	XP_016883959.1:p.Leu162=
XM_017028471.1:c.231G>T	XP_016883960.1:p.Leu77=
XM_017028472.1:c.-43G>T	XP_016883961.1:n.-43G>T
XR_937571.2:n.492G>T
NM_004928.3:c.282G>T MANE Select	NP_004919.1:p.Leu94=
NM_001271440.2:c.282G>T	NP_001258369.1:p.Leu94=
NM_001271441.2:c.282G>T	NP_001258370.1:p.Leu94=