Canonical Allele Identifier: CA821649995
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1341337414
MyVariant Identifiers: chr6:g.1612745_1612746del (hg19) chr6:g.1612510_1612511del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612512_1612513del , CM000668.2:g.1612512_1612513del GRCh38
NC_000006.11:g.1612747_1612748del , CM000668.1:g.1612747_1612748del GRCh37
NC_000006.10:g.1557746_1557747del NCBI36
NG_009368.1:g.7067_7068del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*405_*406del MANE Select ENSP00000493906.1:n.*405_*406del
ENST00000380874.3:c.*405_*406del ENSP00000370256.2:n.*405_*406del
NM_001453.2:c.2067_2068del NP_001444.2:n.2067_2068del
NM_001453.3:c.*405_*406del MANE Select NP_001444.2:n.*405_*406del
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