Canonical Allele Identifier: CA891862925

Gene: CFAP43

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104140592_104143904del , CM000672.2:g.104140592_104143904del	GRCh38
NC_000010.10:g.105900350_105903662del , CM000672.1:g.105900350_105903662del	GRCh37
NC_000010.9:g.105890340_105893652del	NCBI36
NG_051581.1:g.93476_96788del

Transcript Alleles

HGVS	Amino-acid Change
NM_025145.5:c.3945-263_4431+252del
NM_025145.6:c.3945-263_4431+252del
NM_025145.7:c.3945-263_4431+252del
ENST00000357060.7:c.3945-263_4431+252del
ENST00000357060.8:c.3945-263_4431+252del
ENST00000434629.5:c.1940-263_2426+252del
ENST00000457071.5:c.491-263_977+252del
XM_005270171.1:c.3948-263_4434+252del
XM_005270171.2:c.3948-263_4434+252del
XM_005270172.2:c.3861-263_4347+252del
XM_005270172.3:c.3861-263_4347+252del
XM_011540196.1:c.4062-263_4548+252del
XM_011540196.2:c.4062-263_4548+252del
XM_011540197.1:c.3975-263_4461+252del
XM_011540197.2:c.3975-263_4461+252del
XM_011540198.1:c.3945-263_4431+252del
XM_011540198.2:c.3945-263_4431+252del
XM_011540199.1:c.3945-263_4431+252del
XM_011540199.2:c.3945-263_4431+252del
XM_011540200.1:c.3778-1509_4050+252del
XM_011540200.2:c.3778-1509_4050+252del
XM_011540201.1:c.4062-263_4548+252del
XM_011540201.2:c.4062-263_4548+252del
XM_011540202.1:c.3291-263_3777+252del
XM_011540202.2:c.3291-263_3777+252del
XM_011540203.1:c.1845-263_2331+252del
XM_017016681.1:c.4059-263_4545+252del
XM_017016682.1:c.3714-263_4200+252del
XM_024448177.1:c.2448-263_2934+252del
XM_024448178.1:c.1845-263_2331+252del
XR_002957015.1:n.6070-263_6556+252del