Canonical Allele Identifier: CA1803867865
Gene: CFAP418 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95247612C= , CM000670.2:g.95247612C= GRCh38
NC_000008.10:g.96259840C= , CM000670.1:g.96259840C= GRCh37
NC_000008.9:g.96329016C= NCBI36
NG_032804.1:g.26623G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.*5G= MANE Select ENSP00000286688.5:n.*5G=
ENST00000286688.5:c.*5G= ENSP00000286688.5:n.*5G=
NM_177965.3:c.*5G= NP_808880.1:n.*5G=
XM_005250799.2:c.*5G= XP_005250856.2:n.*5G=
NM_001363260.1:c.*5G= NP_001350189.1:n.*5G=
NM_177965.4:c.*5G= MANE Select NP_808880.1:n.*5G=