Canonical Allele Identifier: CA2140897082
Gene: SIX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645043A= , CM000676.2:g.60645043A= GRCh38
NC_000014.8:g.61111761A= , CM000676.1:g.61111761A= GRCh37
NC_000014.7:g.60181514A= NCBI36
NG_008231.1:g.9395T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*1240T= MANE Select ENSP00000494686.1:n.*1240T=
ENST00000247182.6:c.*1240T= ENSP00000247182.5:n.*1240T=
ENST00000554986.2:c.*1240T= ENSP00000452700.2:n.*1240T=
ENST00000555955.3:n.2732T=
NM_005982.3:c.*1240T= NP_005973.1:n.*1240T=
XM_017021602.2:c.*1514T= XP_016877091.1:n.*1514T=
NM_005982.4:c.*1240T= MANE Select NP_005973.1:n.*1240T=
Search 100 bp 5'
Search 100 bp 3'