Canonical Allele Identifier: CA1933460208
Gene: CFAP43 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104162328G= , CM000672.2:g.104162328G= GRCh38
NC_000010.10:g.105922086G= , CM000672.1:g.105922086G= GRCh37
NC_000010.9:g.105912076G= NCBI36
NG_051581.1:g.75050C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000357060.8:c.3322C= MANE Select ENSP00000349568.3:p.Leu1108=
ENST00000357060.7:c.3322C= ENSP00000349568.3:p.Leu1108=
ENST00000434629.5:c.1404C=
NM_025145.5:c.3322C= NP_079421.5:p.Leu1108=
XM_005270171.1:c.3325C= XP_005270228.1:p.Leu1109=
XM_005270172.2:c.3325C= XP_005270229.1:p.Leu1109=
XM_011540196.1:c.3439C= XP_011538498.1:p.Leu1147=
XM_011540197.1:c.3439C= XP_011538499.1:p.Leu1147=
XM_011540198.1:c.3322C= XP_011538500.1:p.Leu1108=
XM_011540199.1:c.3322C= XP_011538501.1:p.Leu1108=
XM_011540200.1:c.3439C= XP_011538502.1:p.Leu1147=
XM_011540201.1:c.3439C= XP_011538503.1:p.Leu1147=
XM_011540202.1:c.2668C= XP_011538504.1:p.Leu890=
XM_011540203.1:c.1222C= XP_011538505.1:p.Leu408=
NM_025145.6:c.3322C= NP_079421.5:p.Leu1108=
XM_005270171.2:c.3325C= XP_005270228.1:p.Leu1109=
XM_005270172.3:c.3325C= XP_005270229.1:p.Leu1109=
XM_011540196.2:c.3439C= XP_011538498.1:p.Leu1147=
XM_011540197.2:c.3439C= XP_011538499.1:p.Leu1147=
XM_011540198.2:c.3322C= XP_011538500.1:p.Leu1108=
XM_011540199.2:c.3322C= XP_011538501.1:p.Leu1108=
XM_011540200.2:c.3439C= XP_011538502.1:p.Leu1147=
XM_011540201.2:c.3439C= XP_011538503.1:p.Leu1147=
XM_011540202.2:c.2668C= XP_011538504.1:p.Leu890=
XM_017016681.1:c.3436C= XP_016872170.1:p.Leu1146=
XM_017016682.1:c.3091C= XP_016872171.1:p.Leu1031=
XM_024448177.1:c.1825C= XP_024303945.1:p.Leu609=
XM_024448178.1:c.1222C= XP_024303946.1:p.Leu408=
XR_002957015.1:n.3208C=
NM_025145.7:c.3322C= MANE Select NP_079421.5:p.Leu1108=