Canonical Allele Identifier: CA2140879259
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60648635C= , CM000676.2:g.60648635C= GRCh38
NC_000014.8:g.61115353C= , CM000676.1:g.61115353C= GRCh37
NC_000014.7:g.60185106C= NCBI36
NG_008231.1:g.5803G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.555G= MANE Select ENSP00000494686.1:p.Lys185=
ENST00000247182.6:c.555G= ENSP00000247182.5:p.Lys185=
ENST00000553535.2:n.249-2058G=
ENST00000554986.2:c.42-2058G= ENSP00000452700.2:n.42-2058G=
ENST00000555955.3:n.1198-2058G=
NM_005982.3:c.555G= NP_005973.1:p.Lys185=
XM_017021602.2:c.501+54G= XP_016877091.1:n.501+54G=
NM_005982.4:c.555G= MANE Select NP_005973.1:p.Lys185=