Canonical Allele Identifier: CA2769749160
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612622_1612623insACA , CM000668.2:g.1612622_1612623insACA GRCh38
NC_000006.11:g.1612857_1612858insACA , CM000668.1:g.1612857_1612858insACA GRCh37
NC_000006.10:g.1557856_1557857insACA NCBI36
NG_009368.1:g.7177_7178insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*515_*516insACA MANE Select ENSP00000493906.1:n.*515_*516insACA
ENST00000380874.3:c.*515_*516insACA ENSP00000370256.2:n.*515_*516insACA
NM_001453.2:c.2177_2178insACA NP_001444.2:n.2177_2178insACA
NM_001453.3:c.*515_*516insACA MANE Select NP_001444.2:n.*515_*516insACA