Canonical Allele Identifier: CA2140879249
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60648632T= , CM000676.2:g.60648632T= GRCh38
NC_000014.8:g.61115350T= , CM000676.1:g.61115350T= GRCh37
NC_000014.7:g.60185103T= NCBI36
NG_008231.1:g.5806A=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.558A= MANE Select ENSP00000494686.1:p.Glu186=
ENST00000247182.6:c.558A= ENSP00000247182.5:p.Glu186=
ENST00000553535.2:n.249-2055A=
ENST00000554986.2:c.42-2055A= ENSP00000452700.2:n.42-2055A=
ENST00000555955.3:n.1198-2055A=
NM_005982.3:c.558A= NP_005973.1:p.Glu186=
XM_017021602.2:c.501+57A= XP_016877091.1:n.501+57A=
NM_005982.4:c.558A= MANE Select NP_005973.1:p.Glu186=