Canonical Allele Identifier: CA378091929
Gene: CFAP43 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.104162025A>T , CM000672.2:g.104162025A>T GRCh38
NC_000010.10:g.105921783A>T , CM000672.1:g.105921783A>T GRCh37
NC_000010.9:g.105911773A>T NCBI36
NG_051581.1:g.75353T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000357060.8:c.3350T>A MANE Select ENSP00000349568.3:p.Leu1117His
ENST00000357060.7:c.3350T>A ENSP00000349568.3:p.Leu1117His
ENST00000434629.5:c.1432T>A
NM_025145.5:c.3350T>A NP_079421.5:p.Leu1117His
XM_005270171.1:c.3353T>A XP_005270228.1:p.Leu1118His
XM_005270172.2:c.3353T>A XP_005270229.1:p.Leu1118His
XM_011540196.1:c.3467T>A XP_011538498.1:p.Leu1156His
XM_011540197.1:c.3467T>A XP_011538499.1:p.Leu1156His
XM_011540198.1:c.3350T>A XP_011538500.1:p.Leu1117His
XM_011540199.1:c.3350T>A XP_011538501.1:p.Leu1117His
XM_011540200.1:c.3467T>A XP_011538502.1:p.Leu1156His
XM_011540201.1:c.3467T>A XP_011538503.1:p.Leu1156His
XM_011540202.1:c.2696T>A XP_011538504.1:p.Leu899His
XM_011540203.1:c.1250T>A XP_011538505.1:p.Leu417His
NM_025145.6:c.3350T>A NP_079421.5:p.Leu1117His
XM_005270171.2:c.3353T>A XP_005270228.1:p.Leu1118His
XM_005270172.3:c.3353T>A XP_005270229.1:p.Leu1118His
XM_011540196.2:c.3467T>A XP_011538498.1:p.Leu1156His
XM_011540197.2:c.3467T>A XP_011538499.1:p.Leu1156His
XM_011540198.2:c.3350T>A XP_011538500.1:p.Leu1117His
XM_011540199.2:c.3350T>A XP_011538501.1:p.Leu1117His
XM_011540200.2:c.3467T>A XP_011538502.1:p.Leu1156His
XM_011540201.2:c.3467T>A XP_011538503.1:p.Leu1156His
XM_011540202.2:c.2696T>A XP_011538504.1:p.Leu899His
XM_017016681.1:c.3464T>A XP_016872170.1:p.Leu1155His
XM_017016682.1:c.3119T>A XP_016872171.1:p.Leu1040His
XM_024448177.1:c.1853T>A XP_024303945.1:p.Leu618His
XM_024448178.1:c.1250T>A XP_024303946.1:p.Leu417His
XR_002957015.1:n.3236T>A
NM_025145.7:c.3350T>A MANE Select NP_079421.5:p.Leu1117His