Canonical Allele Identifier: CA1866669542
Gene: FOXE1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853898T= , CM000671.2:g.97853898T= GRCh38
NC_000009.11:g.100616180T= , CM000671.1:g.100616180T= GRCh37
NC_000009.10:g.99656001T= NCBI36
NG_011979.1:g.5644T=

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.-17T= MANE Select ENSP00000364265.3:n.-17T=
ENST00000375123.4:c.-17T= ENSP00000364265.3:n.-17T=
NM_004473.3:c.-17T= NP_004464.2:n.-17T=
NM_004473.4:c.-17T= MANE Select NP_004464.2:n.-17T=
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