Canonical Allele Identifier: CA348502957
Gene: CFC1 HGNC NCBI

Linked Data

dbSNP Id: rs1373655103

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.130593055G>C , CM000664.2:g.130593055G>C GRCh38
NC_000002.11:g.131350628G>C , CM000664.1:g.131350628G>C GRCh37
NC_000002.10:g.131067098G>C NCBI36
NG_008148.1:g.11455C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259216.6:c.494C>G MANE Select ENSP00000259216.5:p.Ser165Cys
ENST00000259216.4:c.494C>G ENSP00000259216.4:p.Ser165Cys
ENST00000615342.4:c.379C>G ENSP00000480526.1:p.Pro127Ala
ENST00000621673.4:c.269C>G ENSP00000480843.1:p.Ser90Cys
NM_001270420.1:c.379C>G NP_001257349.1:p.Pro127Ala
NM_001270421.1:c.269C>G NP_001257350.1:p.Ser90Cys
NM_032545.3:c.494C>G NP_115934.1:p.Ser165Cys
NM_032545.4:c.494C>G MANE Select NP_115934.1:p.Ser165Cys
NM_001270420.2:c.379C>G NP_001257349.1:p.Pro127Ala
NM_001270421.2:c.269C>G NP_001257350.1:p.Ser90Cys