Canonical Allele Identifier: CA2769749178
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612809_1612810insA , CM000668.2:g.1612809_1612810insA GRCh38
NC_000006.11:g.1613044_1613045insA , CM000668.1:g.1613044_1613045insA GRCh37
NC_000006.10:g.1558043_1558044insA NCBI36
NG_009368.1:g.7364_7365insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*702_*703insA MANE Select ENSP00000493906.1:n.*702_*703insA
ENST00000380874.3:c.*702_*703insA ENSP00000370256.2:n.*702_*703insA
NM_001453.2:c.2364_2365insA NP_001444.2:n.2364_2365insA
NM_001453.3:c.*702_*703insA MANE Select NP_001444.2:n.*702_*703insA