Canonical Allele Identifier: CA389475596

Gene: FOXG1

Linked Data

• MyVariant Identifiers: chr14:g.29237147A>C (hg19) ; chr14:g.28767941A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.28767941A>C , CM000676.2:g.28767941A>C	GRCh38
NC_000014.8:g.29237147A>C , CM000676.1:g.29237147A>C	GRCh37
NC_000014.7:g.28306898A>C	NCBI36
NG_009367.1:g.5861A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706482.1:c.662A>C	ENSP00000516406.1:p.Asn221Thr
ENST00000313071.7:c.662A>C MANE Select	ENSP00000339004.3:p.Asn221Thr
ENST00000313071.6:c.662A>C	ENSP00000339004.3:p.Asn221Thr
NM_005249.4:c.662A>C	NP_005240.3:p.Asn221Thr
NM_005249.5:c.662A>C MANE Select	NP_005240.3:p.Asn221Thr