Canonical Allele Identifier: CA2140882129
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649444C= , CM000676.2:g.60649444C= GRCh38
NC_000014.8:g.61116162C= , CM000676.1:g.61116162C= GRCh37
NC_000014.7:g.60185915C= NCBI36
NG_008231.1:g.4994G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.-255G= MANE Select ENSP00000494686.1:n.-255G=
ENST00000247182.6:c.-255G= ENSP00000247182.5:n.-255G=
ENST00000553535.2:n.248+2491G=
ENST00000554986.2:c.42-2867G= ENSP00000452700.2:n.42-2867G=
ENST00000555955.3:n.1197+2491G=
XM_017021602.2:c.-255G= XP_016877091.1:n.-255G=
NM_005982.4:c.-255G= MANE Select NP_005973.1:n.-255G=