Canonical Allele Identifier: CA2624398553
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767507_28767508insTCTA , CM000676.2:g.28767507_28767508insTCTA GRCh38
NC_000014.8:g.29236713_29236714insTCTA , CM000676.1:g.29236713_29236714insTCTA GRCh37
NC_000014.7:g.28306464_28306465insTCTA NCBI36
NG_009367.1:g.5427_5428insTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.228_229insTCTA ENSP00000516406.1:p.Pro77SerfsTer?
ENST00000313071.7:c.228_229insTCTA MANE Select ENSP00000339004.3:p.Pro77SerfsTer?
ENST00000313071.6:c.228_229insTCTA ENSP00000339004.3:p.Pro77SerfsTer?
NM_005249.4:c.228_229insTCTA NP_005240.3:p.Pro77SerfsTer?
NM_005249.5:c.228_229insTCTA MANE Select NP_005240.3:p.Pro77SerfsTer?