Canonical Allele Identifier: CA2125998863
Gene: FOXG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28767485_28767491delinsCGCAGCA , CM000676.2:g.28767485_28767491delinsCGCAGCA GRCh38
NC_000014.8:g.29236691_29236697delinsCGCAGCA , CM000676.1:g.29236691_29236697delinsCGCAGCA GRCh37
NC_000014.7:g.28306442_28306448delinsCGCAGCA NCBI36
NG_009367.1:g.5405_5411delinsCGCAGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.206_212delinsCGCAGCA ENSP00000516406.1:p.Pro69=
ENST00000313071.7:c.206_212delinsCGCAGCA MANE Select ENSP00000339004.3:p.Pro69=
ENST00000313071.6:c.206_212delinsCGCAGCA ENSP00000339004.3:p.Pro69=
NM_005249.4:c.206_212delinsCGCAGCA NP_005240.3:p.Pro69=
NM_005249.5:c.206_212delinsCGCAGCA MANE Select NP_005240.3:p.Pro69=
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