Canonical Allele Identifier: CA389475712

Gene: FOXG1

Linked Data

• MyVariant Identifiers: chr14:g.29237201T>C (hg19) ; chr14:g.28767995T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28767995T>C , CM000676.2:g.28767995T>C	GRCh38
NC_000014.8:g.29237201T>C , CM000676.1:g.29237201T>C	GRCh37
NC_000014.7:g.28306952T>C	NCBI36
NG_009367.1:g.5915T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.716T>C	ENSP00000516406.1:p.Phe239Ser
ENST00000313071.7:c.716T>C MANE Select	ENSP00000339004.3:p.Phe239Ser
ENST00000313071.6:c.716T>C	ENSP00000339004.3:p.Phe239Ser
NM_005249.4:c.716T>C	NP_005240.3:p.Phe239Ser
NM_005249.5:c.716T>C MANE Select	NP_005240.3:p.Phe239Ser