Canonical Allele Identifier: CA18103412
Gene: CFAP107 HGNC NCBI

Linked Data

dbSNP Id: rs141882357
gnomAD v4: 1-12746532-G-A
COSMIC: COSM109914

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12746532G>A , CM000663.2:g.12746532G>A GRCh38
NC_000001.10:g.12806480G>A , CM000663.1:g.12806480G>A GRCh37
NC_000001.9:g.12729067G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000614859.5:c.102G>A MANE Select ENSP00000477802.1:p.Glu34=
ENST00000376210.3:c.102G>A ENSP00000365383.3:p.Glu34=
ENST00000474179.1:n.146G>A
ENST00000614859.4:c.102G>A ENSP00000477802.1:p.Glu34=
NM_152290.3:c.102G>A NP_689503.3:p.Glu34=
XM_011542434.1:c.102G>A XP_011540736.1:p.Glu34=
NM_001330361.1:c.102G>A NP_001317290.1:p.Glu34=
NM_152290.4:c.102G>A MANE Select NP_689503.3:p.Glu34=
NM_001330361.2:c.102G>A NP_001317290.1:p.Glu34=