Canonical Allele Identifier: CA2140881975
Gene: SIX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649402G= , CM000676.2:g.60649402G= GRCh38
NC_000014.8:g.61116120G= , CM000676.1:g.61116120G= GRCh37
NC_000014.7:g.60185873G= NCBI36
NG_008231.1:g.5036C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.-213C= MANE Select ENSP00000494686.1:n.-213C=
ENST00000247182.6:c.-213C= ENSP00000247182.5:n.-213C=
ENST00000553535.2:n.248+2533C=
ENST00000554986.2:c.42-2825C= ENSP00000452700.2:n.42-2825C=
ENST00000555955.3:n.1197+2533C=
NM_005982.3:c.-213C= NP_005973.1:n.-213C=
XM_017021602.2:c.-213C= XP_016877091.1:n.-213C=
NM_005982.4:c.-213C= MANE Select NP_005973.1:n.-213C=
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