Canonical Allele Identifier: CA348502385

Gene: CFC1

Linked Data

• MyVariant Identifiers: chr2:g.131350527G>C (hg19) ; chr2:g.130592954G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.130592954G>C , CM000664.2:g.130592954G>C	GRCh38
NC_000002.11:g.131350527G>C , CM000664.1:g.131350527G>C	GRCh37
NC_000002.10:g.131066997G>C	NCBI36
NG_008148.1:g.11556C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000259216.6:c.595C>G MANE Select	ENSP00000259216.5:p.Pro199Ala
ENST00000259216.4:c.595C>G	ENSP00000259216.4:p.Pro199Ala
ENST00000615342.4:c.480C>G	ENSP00000480526.1:p.Thr160=
ENST00000621673.4:c.370C>G	ENSP00000480843.1:p.Pro124Ala
NM_001270420.1:c.480C>G	NP_001257349.1:p.Thr160=
NM_001270421.1:c.370C>G	NP_001257350.1:p.Pro124Ala
NM_032545.3:c.595C>G	NP_115934.1:p.Pro199Ala
NM_032545.4:c.595C>G MANE Select	NP_115934.1:p.Pro199Ala
NM_001270420.2:c.480C>G	NP_001257349.1:p.Thr160=
NM_001270421.2:c.370C>G	NP_001257350.1:p.Pro124Ala