Canonical Allele Identifier: CA1085282060
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609996_1609997insACTC , CM000668.2:g.1609996_1609997insACTC GRCh38
NC_000006.11:g.1610231_1610232insACTC , CM000668.1:g.1610231_1610232insACTC GRCh37
NC_000006.10:g.1555230_1555231insACTC NCBI36
NG_009368.1:g.4551_4552insACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-450_-449insACTC MANE Select ENSP00000493906.1:n.-450_-449insACTC
ENST00000380874.3:c.-450_-449insACTC ENSP00000370256.2:n.-450_-449insACTC
NM_001453.3:c.-450_-449insACTC MANE Select NP_001444.2:n.-450_-449insACTC