Canonical Allele Identifier: CA2677060377
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610407_1610413del , CM000668.2:g.1610407_1610413del GRCh38
NC_000006.11:g.1610642_1610648del , CM000668.1:g.1610642_1610648del GRCh37
NC_000006.10:g.1555641_1555647del NCBI36
NG_009368.1:g.4962_4968del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-39_-33del MANE Select ENSP00000493906.1:n.-39_-33del
ENST00000380874.3:c.-39_-33del ENSP00000370256.2:n.-39_-33del
NM_001453.3:c.-39_-33del MANE Select NP_001444.2:n.-39_-33del