Canonical Allele Identifier: CA389475823

Gene: FOXG1

Linked Data

• MyVariant Identifiers: chr14:g.29237251A>G (hg19) ; chr14:g.28768045A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28768045A>G , CM000676.2:g.28768045A>G	GRCh38
NC_000014.8:g.29237251A>G , CM000676.1:g.29237251A>G	GRCh37
NC_000014.7:g.28307002A>G	NCBI36
NG_009367.1:g.5965A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.766A>G	ENSP00000516406.1:p.Met256Val
ENST00000313071.7:c.766A>G MANE Select	ENSP00000339004.3:p.Met256Val
ENST00000313071.6:c.766A>G	ENSP00000339004.3:p.Met256Val
NM_005249.4:c.766A>G	NP_005240.3:p.Met256Val
NM_005249.5:c.766A>G MANE Select	NP_005240.3:p.Met256Val