Canonical Allele Identifier: CA1605823688
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612795T= , CM000668.2:g.1612795T= GRCh38
NC_000006.11:g.1613030T= , CM000668.1:g.1613030T= GRCh37
NC_000006.10:g.1558029T= NCBI36
NG_009368.1:g.7350T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*688T= MANE Select ENSP00000493906.1:n.*688T=
ENST00000380874.3:c.*688T= ENSP00000370256.2:n.*688T=
NM_001453.2:c.2350T= NP_001444.2:n.2350T=
NM_001453.3:c.*688T= MANE Select NP_001444.2:n.*688T=