Canonical Allele Identifier: CA471342255

Gene: CFAP43

Linked Data

• MyVariant Identifiers: chr10:g.105921776A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104162018A>C , CM000672.2:g.104162018A>C	GRCh38
NC_000010.10:g.105921776A>C , CM000672.1:g.105921776A>C	GRCh37
NC_000010.9:g.105911766A>C	NCBI36
NG_051581.1:g.75360T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357060.8:c.3357T>G MANE Select	ENSP00000349568.3:p.Ala1119=
ENST00000357060.7:c.3357T>G	ENSP00000349568.3:p.Ala1119=
ENST00000434629.5:c.1439T>G
NM_025145.5:c.3357T>G	NP_079421.5:p.Ala1119=
XM_005270171.1:c.3360T>G	XP_005270228.1:p.Ala1120=
XM_005270172.2:c.3360T>G	XP_005270229.1:p.Ala1120=
XM_011540196.1:c.3474T>G	XP_011538498.1:p.Ala1158=
XM_011540197.1:c.3474T>G	XP_011538499.1:p.Ala1158=
XM_011540198.1:c.3357T>G	XP_011538500.1:p.Ala1119=
XM_011540199.1:c.3357T>G	XP_011538501.1:p.Ala1119=
XM_011540200.1:c.3474T>G	XP_011538502.1:p.Ala1158=
XM_011540201.1:c.3474T>G	XP_011538503.1:p.Ala1158=
XM_011540202.1:c.2703T>G	XP_011538504.1:p.Ala901=
XM_011540203.1:c.1257T>G	XP_011538505.1:p.Ala419=
NM_025145.6:c.3357T>G	NP_079421.5:p.Ala1119=
XM_005270171.2:c.3360T>G	XP_005270228.1:p.Ala1120=
XM_005270172.3:c.3360T>G	XP_005270229.1:p.Ala1120=
XM_011540196.2:c.3474T>G	XP_011538498.1:p.Ala1158=
XM_011540197.2:c.3474T>G	XP_011538499.1:p.Ala1158=
XM_011540198.2:c.3357T>G	XP_011538500.1:p.Ala1119=
XM_011540199.2:c.3357T>G	XP_011538501.1:p.Ala1119=
XM_011540200.2:c.3474T>G	XP_011538502.1:p.Ala1158=
XM_011540201.2:c.3474T>G	XP_011538503.1:p.Ala1158=
XM_011540202.2:c.2703T>G	XP_011538504.1:p.Ala901=
XM_017016681.1:c.3471T>G	XP_016872170.1:p.Ala1157=
XM_017016682.1:c.3126T>G	XP_016872171.1:p.Ala1042=
XM_024448177.1:c.1860T>G	XP_024303945.1:p.Ala620=
XM_024448178.1:c.1257T>G	XP_024303946.1:p.Ala419=
XR_002957015.1:n.3243T>G
NM_025145.7:c.3357T>G MANE Select	NP_079421.5:p.Ala1119=