Canonical Allele Identifier: CA869022059
Gene: FOXE1 HGNC NCBI

Linked Data

dbSNP Id: rs71369530

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97854443_97854451dup , CM000671.2:g.97854443_97854451dup GRCh38
NC_000009.11:g.100616725_100616733dup , CM000671.1:g.100616725_100616733dup GRCh37
NC_000009.10:g.99656546_99656554dup NCBI36
NG_011979.1:g.6189_6197dup

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.529_537dup MANE Select ENSP00000364265.3:p.Ala179_Ile180insAlaAl...
ENST00000375123.4:c.529_537dup ENSP00000364265.3:p.Ala179_Ile180insAlaAl...
NM_004473.3:c.529_537dup NP_004464.2:p.Ala179_Ile180insAlaAlaAla
NM_004473.4:c.529_537dup MANE Select NP_004464.2:p.Ala179_Ile180insAlaAlaAla