Canonical Allele Identifier: CA348502955

Gene: CFC1

Linked Data

• MyVariant Identifiers: chr2:g.131350628G>T (hg19) ; chr2:g.130593055G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259216.6:c.494C>A MANE Select	ENSP00000259216.5:p.Ser165Tyr
ENST00000259216.4:c.494C>A	ENSP00000259216.4:p.Ser165Tyr
ENST00000615342.4:c.379C>A	ENSP00000480526.1:p.Pro127Thr
ENST00000621673.4:c.269C>A	ENSP00000480843.1:p.Ser90Tyr
NM_001270420.1:c.379C>A	NP_001257349.1:p.Pro127Thr
NM_001270421.1:c.269C>A	NP_001257350.1:p.Ser90Tyr
NM_032545.3:c.494C>A	NP_115934.1:p.Ser165Tyr
NM_032545.4:c.494C>A MANE Select	NP_115934.1:p.Ser165Tyr
NM_001270420.2:c.379C>A	NP_001257349.1:p.Pro127Thr
NM_001270421.2:c.269C>A	NP_001257350.1:p.Ser90Tyr