Canonical Allele Identifier: CA2677060904
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612445_1612459dup , CM000668.2:g.1612445_1612459dup GRCh38
NC_000006.11:g.1612680_1612694dup , CM000668.1:g.1612680_1612694dup GRCh37
NC_000006.10:g.1557679_1557693dup NCBI36
NG_009368.1:g.7000_7014dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*338_*352dup MANE Select ENSP00000493906.1:n.*338_*352dup
ENST00000380874.3:c.*338_*352dup ENSP00000370256.2:n.*338_*352dup
NM_001453.2:c.2000_2014dup NP_001444.2:n.2000_2014dup
NM_001453.3:c.*338_*352dup MANE Select NP_001444.2:n.*338_*352dup