Canonical Allele Identifier: CA2677060382
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610414_1610416del , CM000668.2:g.1610414_1610416del GRCh38
NC_000006.11:g.1610649_1610651del , CM000668.1:g.1610649_1610651del GRCh37
NC_000006.10:g.1555648_1555650del NCBI36
NG_009368.1:g.4969_4971del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-32_-30del MANE Select ENSP00000493906.1:n.-32_-30del
ENST00000380874.3:c.-32_-30del ENSP00000370256.2:n.-32_-30del
NM_001453.3:c.-32_-30del MANE Select NP_001444.2:n.-32_-30del