Canonical Allele Identifier: CA512670837

Gene: CFAP410

Linked Data

• MyVariant Identifiers: chr21:g.45752941C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.44333058C>G , CM000683.2:g.44333058C>G	GRCh38
NC_000021.8:g.45752941C>G , CM000683.1:g.45752941C>G	GRCh37
NC_000021.7:g.44577369C>G	NCBI36
NG_032952.1:g.11345G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339818.9:c.348G>C MANE Select	ENSP00000344566.4:p.Pro116=
ENST00000325223.7:c.348G>C	ENSP00000317302.7:p.Pro116=
ENST00000339818.8:c.348G>C	ENSP00000344566.4:p.Pro116=
ENST00000397956.7:c.348G>C	ENSP00000381047.3:p.Pro116=
ENST00000462742.1:n.2519G>C
ENST00000478674.1:n.407G>C
ENST00000496321.5:n.464G>C
NM_001271440.1:c.348G>C	NP_001258369.1:p.Pro116=
NM_001271441.1:c.348G>C	NP_001258370.1:p.Pro116=
NM_001271442.1:c.225G>C	NP_001258371.1:p.Pro75=
NM_004928.2:c.348G>C	NP_004919.1:p.Pro116=
XM_006724051.2:c.423G>C	XP_006724114.1:p.Pro141=
XM_006724052.2:c.423G>C	XP_006724115.1:p.Pro141=
XM_006724053.2:c.24G>C	XP_006724116.1:p.Pro8=
XR_937571.1:n.551G>C
XM_006724051.3:c.423G>C	XP_006724114.1:p.Pro141=
XM_006724053.3:c.24G>C	XP_006724116.1:p.Pro8=
XM_017028470.1:c.552G>C	XP_016883959.1:p.Pro184=
XM_017028471.1:c.297G>C	XP_016883960.1:p.Pro99=
XM_017028472.1:c.24G>C	XP_016883961.1:p.Pro8=
XR_937571.2:n.558G>C
NM_004928.3:c.348G>C MANE Select	NP_004919.1:p.Pro116=
NM_001271440.2:c.348G>C	NP_001258369.1:p.Pro116=
NM_001271441.2:c.348G>C	NP_001258370.1:p.Pro116=