Canonical Allele Identifier: CA1288363423
Gene: CFC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.130592851A= , CM000664.2:g.130592851A= GRCh38
NC_000002.11:g.131350424A= , CM000664.1:g.131350424A= GRCh37
NC_000002.10:g.131066894A= NCBI36
NG_008148.1:g.11659T=

Transcript Alleles

HGVS Amino-acid change
ENST00000259216.6:c.*26T= MANE Select ENSP00000259216.5:n.*26T=
ENST00000259216.4:c.*26T= ENSP00000259216.4:n.*26T=
ENST00000615342.4:c.*7T= ENSP00000480526.1:n.*7T=
ENST00000621673.4:c.*26T= ENSP00000480843.1:n.*26T=
NM_001270420.1:c.*7T= NP_001257349.1:n.*7T=
NM_001270421.1:c.*26T= NP_001257350.1:n.*26T=
NM_032545.3:c.*26T= NP_115934.1:n.*26T=
NM_032545.4:c.*26T= MANE Select NP_115934.1:n.*26T=
NM_001270420.2:c.*7T= NP_001257349.1:n.*7T=
NM_001270421.2:c.*26T= NP_001257350.1:n.*26T=