Canonical Allele Identifier: CA1288363466
Gene: CFC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.130592948A= , CM000664.2:g.130592948A= GRCh38
NC_000002.11:g.131350521A= , CM000664.1:g.131350521A= GRCh37
NC_000002.10:g.131066991A= NCBI36
NG_008148.1:g.11562T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259216.6:c.601T= MANE Select ENSP00000259216.5:p.Ser201=
ENST00000259216.4:c.601T= ENSP00000259216.4:p.Ser201=
ENST00000615342.4:c.486T= ENSP00000480526.1:p.Gly162=
ENST00000621673.4:c.376T= ENSP00000480843.1:p.Ser126=
NM_001270420.1:c.486T= NP_001257349.1:p.Gly162=
NM_001270421.1:c.376T= NP_001257350.1:p.Ser126=
NM_032545.3:c.601T= NP_115934.1:p.Ser201=
NM_032545.4:c.601T= MANE Select NP_115934.1:p.Ser201=
NM_001270420.2:c.486T= NP_001257349.1:p.Gly162=
NM_001270421.2:c.376T= NP_001257350.1:p.Ser126=