Canonical Allele Identifier: CA2677060331
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610374_1610414del , CM000668.2:g.1610374_1610414del GRCh38
NC_000006.11:g.1610609_1610649del , CM000668.1:g.1610609_1610649del GRCh37
NC_000006.10:g.1555608_1555648del NCBI36
NG_009368.1:g.4929_4969del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-72_-32del MANE Select ENSP00000493906.1:n.-72_-32del
ENST00000380874.3:c.-72_-32del ENSP00000370256.2:n.-72_-32del
NM_001453.3:c.-72_-32del MANE Select NP_001444.2:n.-72_-32del