Canonical Allele Identifier: CA1605821921
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762501568

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610012_1610025del , CM000668.2:g.1610012_1610025del GRCh38
NC_000006.11:g.1610247_1610260del , CM000668.1:g.1610247_1610260del GRCh37
NC_000006.10:g.1555246_1555259del NCBI36
NG_009368.1:g.4567_4580del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-434_-421del MANE Select ENSP00000493906.1:n.-434_-421del
ENST00000380874.3:c.-434_-421del ENSP00000370256.2:n.-434_-421del
NM_001453.3:c.-434_-421del MANE Select NP_001444.2:n.-434_-421del