Canonical Allele Identifier: CA1933460212
Gene: CFAP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104162329C= , CM000672.2:g.104162329C= GRCh38
NC_000010.10:g.105922087C= , CM000672.1:g.105922087C= GRCh37
NC_000010.9:g.105912077C= NCBI36
NG_051581.1:g.75049G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357060.8:c.3321G= MANE Select ENSP00000349568.3:p.Trp1107=
ENST00000357060.7:c.3321G= ENSP00000349568.3:p.Trp1107=
ENST00000434629.5:c.1403G=
NM_025145.5:c.3321G= NP_079421.5:p.Trp1107=
XM_005270171.1:c.3324G= XP_005270228.1:p.Trp1108=
XM_005270172.2:c.3324G= XP_005270229.1:p.Trp1108=
XM_011540196.1:c.3438G= XP_011538498.1:p.Trp1146=
XM_011540197.1:c.3438G= XP_011538499.1:p.Trp1146=
XM_011540198.1:c.3321G= XP_011538500.1:p.Trp1107=
XM_011540199.1:c.3321G= XP_011538501.1:p.Trp1107=
XM_011540200.1:c.3438G= XP_011538502.1:p.Trp1146=
XM_011540201.1:c.3438G= XP_011538503.1:p.Trp1146=
XM_011540202.1:c.2667G= XP_011538504.1:p.Trp889=
XM_011540203.1:c.1221G= XP_011538505.1:p.Trp407=
NM_025145.6:c.3321G= NP_079421.5:p.Trp1107=
XM_005270171.2:c.3324G= XP_005270228.1:p.Trp1108=
XM_005270172.3:c.3324G= XP_005270229.1:p.Trp1108=
XM_011540196.2:c.3438G= XP_011538498.1:p.Trp1146=
XM_011540197.2:c.3438G= XP_011538499.1:p.Trp1146=
XM_011540198.2:c.3321G= XP_011538500.1:p.Trp1107=
XM_011540199.2:c.3321G= XP_011538501.1:p.Trp1107=
XM_011540200.2:c.3438G= XP_011538502.1:p.Trp1146=
XM_011540201.2:c.3438G= XP_011538503.1:p.Trp1146=
XM_011540202.2:c.2667G= XP_011538504.1:p.Trp889=
XM_017016681.1:c.3435G= XP_016872170.1:p.Trp1145=
XM_017016682.1:c.3090G= XP_016872171.1:p.Trp1030=
XM_024448177.1:c.1824G= XP_024303945.1:p.Trp608=
XM_024448178.1:c.1221G= XP_024303946.1:p.Trp407=
XR_002957015.1:n.3207G=
NM_025145.7:c.3321G= MANE Select NP_079421.5:p.Trp1107=