Canonical Allele Identifier: CA821650134
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1273050921
gnomAD v3: 6-1612799-TAATA-T
gnomAD v4: 6-1612799-TAATA-T
MyVariant Identifiers: chr6:g.1613035_1613038del (hg19) chr6:g.1612800_1612803del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612803_1612806del , CM000668.2:g.1612803_1612806del GRCh38
NC_000006.11:g.1613038_1613041del , CM000668.1:g.1613038_1613041del GRCh37
NC_000006.10:g.1558037_1558040del NCBI36
NG_009368.1:g.7358_7361del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*696_*699del MANE Select ENSP00000493906.1:n.*696_*699del
ENST00000380874.3:c.*696_*699del ENSP00000370256.2:n.*696_*699del
NM_001453.2:c.2358_2361del NP_001444.2:n.2358_2361del
NM_001453.3:c.*696_*699del MANE Select NP_001444.2:n.*696_*699del
Search 100 bp 5'
Search 100 bp 3'