Canonical Allele Identifier: CA118580
Gene: FOXE1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97854218C>T , CM000671.2:g.97854218C>T GRCh38
NC_000009.11:g.100616500C>T , CM000671.1:g.100616500C>T GRCh37
NC_000009.10:g.99656321C>T NCBI36
NG_011979.1:g.5964C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375123.5:c.304C>T MANE Select ENSP00000364265.3:p.Arg102Cys
ENST00000375123.4:c.304C>T ENSP00000364265.3:p.Arg102Cys
NM_004473.3:c.304C>T NP_004464.2:p.Arg102Cys
NM_004473.4:c.304C>T MANE Select NP_004464.2:p.Arg102Cys