Canonical Allele Identifier: CA1085282360
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v3: 6-1610019-C-CA
gnomAD v4: 6-1610019-C-CA

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610019_1610020insA , CM000668.2:g.1610019_1610020insA GRCh38
NC_000006.11:g.1610254_1610255insA , CM000668.1:g.1610254_1610255insA GRCh37
NC_000006.10:g.1555253_1555254insA NCBI36
NG_009368.1:g.4574_4575insA

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-427_-426insA MANE Select ENSP00000493906.1:n.-427_-426insA
ENST00000380874.3:c.-427_-426insA ENSP00000370256.2:n.-427_-426insA
NM_001453.3:c.-427_-426insA MANE Select NP_001444.2:n.-427_-426insA