Canonical Allele Identifier: CA2687988725
Gene: CFAP418 HGNC NCBI

Linked Data

gnomAD v4: 8-95247603-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95247603T>G , CM000670.2:g.95247603T>G GRCh38
NC_000008.10:g.96259831T>G , CM000670.1:g.96259831T>G GRCh37
NC_000008.9:g.96329007T>G NCBI36
NG_032804.1:g.26632A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.*14A>C MANE Select ENSP00000286688.5:n.*14A>C
ENST00000286688.5:c.*14A>C ENSP00000286688.5:n.*14A>C
NM_177965.3:c.*14A>C NP_808880.1:n.*14A>C
XM_005250799.2:c.*14A>C XP_005250856.2:n.*14A>C
NM_001363260.1:c.*14A>C NP_001350189.1:n.*14A>C
NM_177965.4:c.*14A>C MANE Select NP_808880.1:n.*14A>C