Canonical Allele Identifier: CA2677060383
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610416_1610435del , CM000668.2:g.1610416_1610435del GRCh38
NC_000006.11:g.1610651_1610670del , CM000668.1:g.1610651_1610670del GRCh37
NC_000006.10:g.1555650_1555669del NCBI36
NG_009368.1:g.4971_4990del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-30_-11del MANE Select ENSP00000493906.1:n.-30_-11del
ENST00000380874.3:c.-30_-11del ENSP00000370256.2:n.-30_-11del
NM_001453.3:c.-30_-11del MANE Select NP_001444.2:n.-30_-11del