Canonical Allele Identifier: CA1288363476
Gene: CFC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.130592960C= , CM000664.2:g.130592960C= GRCh38
NC_000002.11:g.131350533C= , CM000664.1:g.131350533C= GRCh37
NC_000002.10:g.131067003C= NCBI36
NG_008148.1:g.11550G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259216.6:c.589G= MANE Select ENSP00000259216.5:p.Ala197=
ENST00000259216.4:c.589G= ENSP00000259216.4:p.Ala197=
ENST00000615342.4:c.474G= ENSP00000480526.1:p.Pro158=
ENST00000621673.4:c.364G= ENSP00000480843.1:p.Ala122=
NM_001270420.1:c.474G= NP_001257349.1:p.Pro158=
NM_001270421.1:c.364G= NP_001257350.1:p.Ala122=
NM_032545.3:c.589G= NP_115934.1:p.Ala197=
NM_032545.4:c.589G= MANE Select NP_115934.1:p.Ala197=
NM_001270420.2:c.474G= NP_001257349.1:p.Pro158=
NM_001270421.2:c.364G= NP_001257350.1:p.Ala122=