Canonical Allele Identifier: CA1085282207
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs562673925

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610029_1610030insCCCCCCCCCCCCCCCCCC , CM000668.2:g.1610029_1610030insCCCCCCCCCCCCCCCCCC GRCh38
NC_000006.11:g.1610264_1610265insCCCCCCCCCCCCCCCCCC , CM000668.1:g.1610264_1610265insCCCCCCCCCCCCCCCCCC GRCh37
NC_000006.10:g.1555263_1555264insCCCCCCCCCCCCCCCCCC NCBI36
NG_009368.1:g.4584_4585insCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-417_-416insCCCCCCCCCCCCCCCCCC MANE Select ENSP00000493906.1:n.-417_-416insCCCCCCCCC...
ENST00000380874.3:c.-417_-416insCCCCCCCCCCCCCCCCCC ENSP00000370256.2:n.-417_-416insCCCCCCCCC...
NM_001453.3:c.-417_-416insCCCCCCCCCCCCCCCCCC MANE Select NP_001444.2:n.-417_-416insCCCCCCCCCCCCCCC...