Canonical Allele Identifier: CA2610809180

Gene: CFAP43

Linked Data

• gnomAD v4: 10-104162011-C-CGACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104162011_104162012insGACAT , CM000672.2:g.104162011_104162012insGACAT	GRCh38
NC_000010.10:g.105921769_105921770insGACAT , CM000672.1:g.105921769_105921770insGACAT	GRCh37
NC_000010.9:g.105911759_105911760insGACAT	NCBI36
NG_051581.1:g.75366_75367insATGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3363_3364insATGTC MANE Select	ENSP00000349568.3:p.Asp1122MetfsTer4
ENST00000357060.7:c.3363_3364insATGTC	ENSP00000349568.3:p.Asp1122MetfsTer4
ENST00000434629.5:c.1445_1446insATGTC
NM_025145.5:c.3363_3364insATGTC	NP_079421.5:p.Asp1122MetfsTer4
XM_005270171.1:c.3366_3367insATGTC	XP_005270228.1:p.Asp1123MetfsTer4
XM_005270172.2:c.3366_3367insATGTC	XP_005270229.1:p.Asp1123MetfsTer4
XM_011540196.1:c.3480_3481insATGTC	XP_011538498.1:p.Asp1161MetfsTer4
XM_011540197.1:c.3480_3481insATGTC	XP_011538499.1:p.Asp1161MetfsTer4
XM_011540198.1:c.3363_3364insATGTC	XP_011538500.1:p.Asp1122MetfsTer4
XM_011540199.1:c.3363_3364insATGTC	XP_011538501.1:p.Asp1122MetfsTer4
XM_011540200.1:c.3480_3481insATGTC	XP_011538502.1:p.Asp1161MetfsTer4
XM_011540201.1:c.3480_3481insATGTC	XP_011538503.1:p.Asp1161MetfsTer4
XM_011540202.1:c.2709_2710insATGTC	XP_011538504.1:p.Asp904MetfsTer4
XM_011540203.1:c.1263_1264insATGTC	XP_011538505.1:p.Asp422MetfsTer4
NM_025145.6:c.3363_3364insATGTC	NP_079421.5:p.Asp1122MetfsTer4
XM_005270171.2:c.3366_3367insATGTC	XP_005270228.1:p.Asp1123MetfsTer4
XM_005270172.3:c.3366_3367insATGTC	XP_005270229.1:p.Asp1123MetfsTer4
XM_011540196.2:c.3480_3481insATGTC	XP_011538498.1:p.Asp1161MetfsTer4
XM_011540197.2:c.3480_3481insATGTC	XP_011538499.1:p.Asp1161MetfsTer4
XM_011540198.2:c.3363_3364insATGTC	XP_011538500.1:p.Asp1122MetfsTer4
XM_011540199.2:c.3363_3364insATGTC	XP_011538501.1:p.Asp1122MetfsTer4
XM_011540200.2:c.3480_3481insATGTC	XP_011538502.1:p.Asp1161MetfsTer4
XM_011540201.2:c.3480_3481insATGTC	XP_011538503.1:p.Asp1161MetfsTer4
XM_011540202.2:c.2709_2710insATGTC	XP_011538504.1:p.Asp904MetfsTer4
XM_017016681.1:c.3477_3478insATGTC	XP_016872170.1:p.Asp1160MetfsTer4
XM_017016682.1:c.3132_3133insATGTC	XP_016872171.1:p.Asp1045MetfsTer4
XM_024448177.1:c.1866_1867insATGTC	XP_024303945.1:p.Asp623MetfsTer4
XM_024448178.1:c.1263_1264insATGTC	XP_024303946.1:p.Asp422MetfsTer4
XR_002957015.1:n.3249_3250insATGTC
NM_025145.7:c.3363_3364insATGTC MANE Select	NP_079421.5:p.Asp1122MetfsTer4