Canonical Allele Identifier: CA2140896814
Gene: SIX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60644692C= , CM000676.2:g.60644692C= GRCh38
NC_000014.8:g.61111410C= , CM000676.1:g.61111410C= GRCh37
NC_000014.7:g.60181163C= NCBI36
NG_008231.1:g.9746G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*1591G= MANE Select ENSP00000494686.1:n.*1591G=
ENST00000247182.6:c.*1591G= ENSP00000247182.5:n.*1591G=
NM_005982.4:c.*1591G= MANE Select NP_005973.1:n.*1591G=
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