Canonical Allele Identifier: CA1605821930

Gene: FOXC1

Linked Data

• dbSNP Id: rs1762501757

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610015_1610016insGGGGGGGGG , CM000668.2:g.1610015_1610016insGGGGGGGGG	GRCh38
NC_000006.11:g.1610250_1610251insGGGGGGGGG , CM000668.1:g.1610250_1610251insGGGGGGGGG	GRCh37
NC_000006.10:g.1555249_1555250insGGGGGGGGG	NCBI36
NG_009368.1:g.4570_4571insGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645831.2:c.-431_-430insGGGGGGGGG MANE Select	ENSP00000493906.1:n.-431_-430insGGGGGGGGG
ENST00000380874.3:c.-431_-430insGGGGGGGGG	ENSP00000370256.2:n.-431_-430insGGGGGGGGG
NM_001453.3:c.-431_-430insGGGGGGGGG MANE Select	NP_001444.2:n.-431_-430insGGGGGGGGG