Canonical Allele Identifier: CA378092239

Gene: CFAP43

Linked Data

• MyVariant Identifiers: chr10:g.105922092G>T (hg19) ; chr10:g.104162334G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104162334G>T , CM000672.2:g.104162334G>T	GRCh38
NC_000010.10:g.105922092G>T , CM000672.1:g.105922092G>T	GRCh37
NC_000010.9:g.105912082G>T	NCBI36
NG_051581.1:g.75044C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3316C>A MANE Select	ENSP00000349568.3:p.His1106Asn
ENST00000357060.7:c.3316C>A	ENSP00000349568.3:p.His1106Asn
ENST00000434629.5:c.1398C>A
NM_025145.5:c.3316C>A	NP_079421.5:p.His1106Asn
XM_005270171.1:c.3319C>A	XP_005270228.1:p.His1107Asn
XM_005270172.2:c.3319C>A	XP_005270229.1:p.His1107Asn
XM_011540196.1:c.3433C>A	XP_011538498.1:p.His1145Asn
XM_011540197.1:c.3433C>A	XP_011538499.1:p.His1145Asn
XM_011540198.1:c.3316C>A	XP_011538500.1:p.His1106Asn
XM_011540199.1:c.3316C>A	XP_011538501.1:p.His1106Asn
XM_011540200.1:c.3433C>A	XP_011538502.1:p.His1145Asn
XM_011540201.1:c.3433C>A	XP_011538503.1:p.His1145Asn
XM_011540202.1:c.2662C>A	XP_011538504.1:p.His888Asn
XM_011540203.1:c.1216C>A	XP_011538505.1:p.His406Asn
NM_025145.6:c.3316C>A	NP_079421.5:p.His1106Asn
XM_005270171.2:c.3319C>A	XP_005270228.1:p.His1107Asn
XM_005270172.3:c.3319C>A	XP_005270229.1:p.His1107Asn
XM_011540196.2:c.3433C>A	XP_011538498.1:p.His1145Asn
XM_011540197.2:c.3433C>A	XP_011538499.1:p.His1145Asn
XM_011540198.2:c.3316C>A	XP_011538500.1:p.His1106Asn
XM_011540199.2:c.3316C>A	XP_011538501.1:p.His1106Asn
XM_011540200.2:c.3433C>A	XP_011538502.1:p.His1145Asn
XM_011540201.2:c.3433C>A	XP_011538503.1:p.His1145Asn
XM_011540202.2:c.2662C>A	XP_011538504.1:p.His888Asn
XM_017016681.1:c.3430C>A	XP_016872170.1:p.His1144Asn
XM_017016682.1:c.3085C>A	XP_016872171.1:p.His1029Asn
XM_024448177.1:c.1819C>A	XP_024303945.1:p.His607Asn
XM_024448178.1:c.1216C>A	XP_024303946.1:p.His406Asn
XR_002957015.1:n.3202C>A
NM_025145.7:c.3316C>A MANE Select	NP_079421.5:p.His1106Asn