Canonical Allele Identifier: CA2140897327
Gene: SIX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645401A= , CM000676.2:g.60645401A= GRCh38
NC_000014.8:g.61112119A= , CM000676.1:g.61112119A= GRCh37
NC_000014.7:g.60181872A= NCBI36
NG_008231.1:g.9037T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*882T= MANE Select ENSP00000494686.1:n.*882T=
ENST00000247182.6:c.*882T= ENSP00000247182.5:n.*882T=
ENST00000553535.2:n.1425T=
ENST00000554986.2:c.*882T= ENSP00000452700.2:n.*882T=
ENST00000555955.3:n.2374T=
NM_005982.3:c.*882T= NP_005973.1:n.*882T=
XM_017021602.2:c.*1156T= XP_016877091.1:n.*1156T=
NM_005982.4:c.*882T= MANE Select NP_005973.1:n.*882T=
Search 100 bp 5'
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