Canonical Allele Identifier: CA362558663

Gene: FOXC1

Linked Data

• COSMIC: COSM1075690
• MyVariant Identifiers: chr6:g.1611048A>C (hg19) ; chr6:g.1610813A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610813A>C , CM000668.2:g.1610813A>C	GRCh38
NC_000006.11:g.1611048A>C , CM000668.1:g.1611048A>C	GRCh37
NC_000006.10:g.1556047A>C	NCBI36
NG_009368.1:g.5368A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645831.2:c.368A>C MANE Select	ENSP00000493906.1:p.Gln123Pro
ENST00000380874.3:c.368A>C	ENSP00000370256.2:p.Gln123Pro
NM_001453.2:c.368A>C	NP_001444.2:p.Gln123Pro
NM_001453.3:c.368A>C MANE Select	NP_001444.2:p.Gln123Pro