Canonical Allele Identifier: CA2140879252
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60648634C= , CM000676.2:g.60648634C= GRCh38
NC_000014.8:g.61115352C= , CM000676.1:g.61115352C= GRCh37
NC_000014.7:g.60185105C= NCBI36
NG_008231.1:g.5804G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.556G= MANE Select ENSP00000494686.1:p.Glu186=
ENST00000247182.6:c.556G= ENSP00000247182.5:p.Glu186=
ENST00000553535.2:n.249-2057G=
ENST00000554986.2:c.42-2057G= ENSP00000452700.2:n.42-2057G=
ENST00000555955.3:n.1198-2057G=
NM_005982.3:c.556G= NP_005973.1:p.Glu186=
XM_017021602.2:c.501+55G= XP_016877091.1:n.501+55G=
NM_005982.4:c.556G= MANE Select NP_005973.1:p.Glu186=