Canonical Allele Identifier: CA1605823691
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612798T= , CM000668.2:g.1612798T= GRCh38
NC_000006.11:g.1613033T= , CM000668.1:g.1613033T= GRCh37
NC_000006.10:g.1558032T= NCBI36
NG_009368.1:g.7353T=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*691T= MANE Select ENSP00000493906.1:n.*691T=
ENST00000380874.3:c.*691T= ENSP00000370256.2:n.*691T=
NM_001453.2:c.2353T= NP_001444.2:n.2353T=
NM_001453.3:c.*691T= MANE Select NP_001444.2:n.*691T=
Search 100 bp 5'
Search 100 bp 3'