Canonical Allele Identifier: CA389475683

Gene: FOXG1

Linked Data

• MyVariant Identifiers: chr14:g.29237189T>C (hg19) ; chr14:g.28767983T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28767983T>C , CM000676.2:g.28767983T>C	GRCh38
NC_000014.8:g.29237189T>C , CM000676.1:g.29237189T>C	GRCh37
NC_000014.7:g.28306940T>C	NCBI36
NG_009367.1:g.5903T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.704T>C	ENSP00000516406.1:p.Leu235Pro
ENST00000313071.7:c.704T>C MANE Select	ENSP00000339004.3:p.Leu235Pro
ENST00000313071.6:c.704T>C	ENSP00000339004.3:p.Leu235Pro
NM_005249.4:c.704T>C	NP_005240.3:p.Leu235Pro
NM_005249.5:c.704T>C MANE Select	NP_005240.3:p.Leu235Pro