Canonical Allele Identifier: CA2677060422
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610435-GA-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610436del , CM000668.2:g.1610436del GRCh38
NC_000006.11:g.1610671del , CM000668.1:g.1610671del GRCh37
NC_000006.10:g.1555670del NCBI36
NG_009368.1:g.4991del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-10del MANE Select ENSP00000493906.1:n.-10del
ENST00000380874.3:c.-10del ENSP00000370256.2:n.-10del
NM_001453.3:c.-10del MANE Select NP_001444.2:n.-10del