Canonical Allele Identifier: CA1605821837
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609931_1609933delinsGTT , CM000668.2:g.1609931_1609933delinsGTT GRCh38
NC_000006.11:g.1610166_1610168delinsGTT , CM000668.1:g.1610166_1610168delinsGTT GRCh37
NC_000006.10:g.1555165_1555167delinsGTT NCBI36
NG_009368.1:g.4486_4488delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-515_-513delinsGTT MANE Select ENSP00000493906.1:n.-515_-513delinsGTT
NM_001453.3:c.-515_-513delinsGTT MANE Select NP_001444.2:n.-515_-513delinsGTT
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