Canonical Allele Identifier: CA1605823571
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612540_1612556delinsGGAAAGTCCCCGTTTAT , CM000668.2:g.1612540_1612556delinsGGAAAGTCCCCGTTTAT GRCh38
NC_000006.11:g.1612775_1612791delinsGGAAAGTCCCCGTTTAT , CM000668.1:g.1612775_1612791delinsGGAAAGTCCCCGTTTAT GRCh37
NC_000006.10:g.1557774_1557790delinsGGAAAGTCCCCGTTTAT NCBI36
NG_009368.1:g.7095_7111delinsGGAAAGTCCCCGTTTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*433_*449delinsGGAAAGTCCCCGTTTAT MANE Select ENSP00000493906.1:n.*433_*449delinsGGAAAGTCCCCGTTTAT
ENST00000380874.3:c.*433_*449delinsGGAAAGTCCCCGTTTAT ENSP00000370256.2:n.*433_*449delinsGGAAAGTCCCCGTTTAT
NM_001453.2:c.2095_2111delinsGGAAAGTCCCCGTTTAT NP_001444.2:n.2095_2111delinsGGAAAGTCCCCGTTTAT
NM_001453.3:c.*433_*449delinsGGAAAGTCCCCGTTTAT MANE Select NP_001444.2:n.*433_*449delinsGGAAAGTCCCCGTTTAT