Canonical Allele Identifier: CA389476626
Gene: FOXG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.28768417A>T , CM000676.2:g.28768417A>T GRCh38
NC_000014.8:g.29237623A>T , CM000676.1:g.29237623A>T GRCh37
NC_000014.7:g.28307374A>T NCBI36
NG_009367.1:g.6337A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706482.1:c.1138A>T ENSP00000516406.1:p.Thr380Ser
ENST00000313071.7:c.1138A>T MANE Select ENSP00000339004.3:p.Thr380Ser
ENST00000313071.6:c.1138A>T ENSP00000339004.3:p.Thr380Ser
NM_005249.4:c.1138A>T NP_005240.3:p.Thr380Ser
NM_005249.5:c.1138A>T MANE Select NP_005240.3:p.Thr380Ser