Canonical Allele Identifier: CA1866669529
Gene: FOXE1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853893G= , CM000671.2:g.97853893G= GRCh38
NC_000009.11:g.100616175G= , CM000671.1:g.100616175G= GRCh37
NC_000009.10:g.99655996G= NCBI36
NG_011979.1:g.5639G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375123.5:c.-22G= MANE Select ENSP00000364265.3:n.-22G=
ENST00000375123.4:c.-22G= ENSP00000364265.3:n.-22G=
NM_004473.3:c.-22G= NP_004464.2:n.-22G=
NM_004473.4:c.-22G= MANE Select NP_004464.2:n.-22G=
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