Canonical Allele Identifier: CA1605821890
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609987_1609988delinsCG , CM000668.2:g.1609987_1609988delinsCG GRCh38
NC_000006.11:g.1610222_1610223delinsCG , CM000668.1:g.1610222_1610223delinsCG GRCh37
NC_000006.10:g.1555221_1555222delinsCG NCBI36
NG_009368.1:g.4542_4543delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-459_-458delinsCG MANE Select ENSP00000493906.1:n.-459_-458delinsCG
ENST00000380874.3:c.-459_-458delinsCG ENSP00000370256.2:n.-459_-458delinsCG
NM_001453.3:c.-459_-458delinsCG MANE Select NP_001444.2:n.-459_-458delinsCG