Canonical Allele Identifier: CA371838066
Gene: CFAP418 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.95247621T>A , CM000670.2:g.95247621T>A GRCh38
NC_000008.10:g.96259849T>A , CM000670.1:g.96259849T>A GRCh37
NC_000008.9:g.96329025T>A NCBI36
NG_032804.1:g.26614A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286688.6:c.620A>T MANE Select ENSP00000286688.5:p.His207Leu
ENST00000286688.5:c.620A>T ENSP00000286688.5:p.His207Leu
NM_177965.3:c.620A>T NP_808880.1:p.His207Leu
XM_005250799.2:c.863A>T XP_005250856.2:p.His288Leu
NM_001363260.1:c.524A>T NP_001350189.1:p.His175Leu
NM_177965.4:c.620A>T MANE Select NP_808880.1:p.His207Leu