Canonical Allele Identifier: CA1866669707
Gene: FOXE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853999G= , CM000671.2:g.97853999G= GRCh38
NC_000009.11:g.100616281G= , CM000671.1:g.100616281G= GRCh37
NC_000009.10:g.99656102G= NCBI36
NG_011979.1:g.5745G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.85G= MANE Select ENSP00000364265.3:p.Ala29=
ENST00000375123.4:c.85G= ENSP00000364265.3:p.Ala29=
NM_004473.3:c.85G= NP_004464.2:p.Ala29=
NM_004473.4:c.85G= MANE Select NP_004464.2:p.Ala29=