Canonical Allele Identifier: CA1866669712
Gene: FOXE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97854002G= , CM000671.2:g.97854002G= GRCh38
NC_000009.11:g.100616284G= , CM000671.1:g.100616284G= GRCh37
NC_000009.10:g.99656105G= NCBI36
NG_011979.1:g.5748G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.88G= MANE Select ENSP00000364265.3:p.Gly30=
ENST00000375123.4:c.88G= ENSP00000364265.3:p.Gly30=
NM_004473.3:c.88G= NP_004464.2:p.Gly30=
NM_004473.4:c.88G= MANE Select NP_004464.2:p.Gly30=