Canonical Allele Identifier: CA1803867856
Gene: CFAP418 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95247610T= , CM000670.2:g.95247610T= GRCh38
NC_000008.10:g.96259838T= , CM000670.1:g.96259838T= GRCh37
NC_000008.9:g.96329014T= NCBI36
NG_032804.1:g.26625A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.*7A= MANE Select ENSP00000286688.5:n.*7A=
ENST00000286688.5:c.*7A= ENSP00000286688.5:n.*7A=
NM_177965.3:c.*7A= NP_808880.1:n.*7A=
XM_005250799.2:c.*7A= XP_005250856.2:n.*7A=
NM_001363260.1:c.*7A= NP_001350189.1:n.*7A=
NM_177965.4:c.*7A= MANE Select NP_808880.1:n.*7A=