Canonical Allele Identifier: CA1866669520
Gene: FOXE1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853892_97853893delinsCG , CM000671.2:g.97853892_97853893delinsCG GRCh38
NC_000009.11:g.100616174_100616175delinsCG , CM000671.1:g.100616174_100616175delinsCG GRCh37
NC_000009.10:g.99655995_99655996delinsCG NCBI36
NG_011979.1:g.5638_5639delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.-23_-22delinsCG MANE Select ENSP00000364265.3:n.-23_-22delinsCG
ENST00000375123.4:c.-23_-22delinsCG ENSP00000364265.3:n.-23_-22delinsCG
NM_004473.3:c.-23_-22delinsCG NP_004464.2:n.-23_-22delinsCG
NM_004473.4:c.-23_-22delinsCG MANE Select NP_004464.2:n.-23_-22delinsCG
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