Canonical Allele Identifier: CA148172
Gene: FOXE1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97854446_97854451del , CM000671.2:g.97854446_97854451del GRCh38
NC_000009.11:g.100616728_100616733del , CM000671.1:g.100616728_100616733del GRCh37
NC_000009.10:g.99656549_99656554del NCBI36
NG_011979.1:g.6192_6197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375123.5:c.532_537del MANE Select ENSP00000364265.3:p.Ala178_Ala179del
ENST00000375123.4:c.532_537del ENSP00000364265.3:p.Ala178_Ala179del
NM_004473.3:c.532_537del NP_004464.2:p.Ala178_Ala179del
NM_004473.4:c.532_537del MANE Select NP_004464.2:p.Ala178_Ala179del