Canonical Allele Identifier: CA1288363531
Gene: CFC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.130593045G= , CM000664.2:g.130593045G= GRCh38
NC_000002.11:g.131350618G= , CM000664.1:g.131350618G= GRCh37
NC_000002.10:g.131067088G= NCBI36
NG_008148.1:g.11465C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259216.6:c.504C= MANE Select ENSP00000259216.5:p.His168=
ENST00000259216.4:c.504C= ENSP00000259216.4:p.His168=
ENST00000615342.4:c.389C= ENSP00000480526.1:p.Thr130=
ENST00000621673.4:c.279C= ENSP00000480843.1:p.His93=
NM_001270420.1:c.389C= NP_001257349.1:p.Thr130=
NM_001270421.1:c.279C= NP_001257350.1:p.His93=
NM_032545.3:c.504C= NP_115934.1:p.His168=
NM_032545.4:c.504C= MANE Select NP_115934.1:p.His168=
NM_001270420.2:c.389C= NP_001257349.1:p.Thr130=
NM_001270421.2:c.279C= NP_001257350.1:p.His93=