Canonical Allele Identifier: CA362558741

Gene: FOXC1

Linked Data

• COSMIC: COSM3860169
• MyVariant Identifiers: chr6:g.1611083T>C (hg19) ; chr6:g.1610848T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610848T>C , CM000668.2:g.1610848T>C	GRCh38
NC_000006.11:g.1611083T>C , CM000668.1:g.1611083T>C	GRCh37
NC_000006.10:g.1556082T>C	NCBI36
NG_009368.1:g.5403T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000645831.2:c.403T>C MANE Select	ENSP00000493906.1:p.Cys135Arg
ENST00000380874.3:c.403T>C	ENSP00000370256.2:p.Cys135Arg
NM_001453.2:c.403T>C	NP_001444.2:p.Cys135Arg
NM_001453.3:c.403T>C MANE Select	NP_001444.2:p.Cys135Arg