Canonical Allele Identifier: CA1288363471
Gene: CFC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.130592953G= , CM000664.2:g.130592953G= GRCh38
NC_000002.11:g.131350526G= , CM000664.1:g.131350526G= GRCh37
NC_000002.10:g.131066996G= NCBI36
NG_008148.1:g.11557C=

Transcript Alleles

HGVS Amino-acid change
ENST00000259216.6:c.596C= MANE Select ENSP00000259216.5:p.Pro199=
ENST00000259216.4:c.596C= ENSP00000259216.4:p.Pro199=
ENST00000615342.4:c.481C= ENSP00000480526.1:p.Leu161=
ENST00000621673.4:c.371C= ENSP00000480843.1:p.Pro124=
NM_001270420.1:c.481C= NP_001257349.1:p.Leu161=
NM_001270421.1:c.371C= NP_001257350.1:p.Pro124=
NM_032545.3:c.596C= NP_115934.1:p.Pro199=
NM_032545.4:c.596C= MANE Select NP_115934.1:p.Pro199=
NM_001270420.2:c.481C= NP_001257349.1:p.Leu161=
NM_001270421.2:c.371C= NP_001257350.1:p.Pro124=