Canonical Allele Identifier: CA371838064
Gene: CFAP418 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95247620A>C , CM000670.2:g.95247620A>C GRCh38
NC_000008.10:g.96259848A>C , CM000670.1:g.96259848A>C GRCh37
NC_000008.9:g.96329024A>C NCBI36
NG_032804.1:g.26615T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.621T>G MANE Select ENSP00000286688.5:p.His207Gln
ENST00000286688.5:c.621T>G ENSP00000286688.5:p.His207Gln
NM_177965.3:c.621T>G NP_808880.1:p.His207Gln
XM_005250799.2:c.864T>G XP_005250856.2:p.His288Gln
NM_001363260.1:c.525T>G NP_001350189.1:p.His175Gln
NM_177965.4:c.621T>G MANE Select NP_808880.1:p.His207Gln