Canonical Allele Identifier: CA2140896909
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60644806C= , CM000676.2:g.60644806C= GRCh38
NC_000014.8:g.61111524C= , CM000676.1:g.61111524C= GRCh37
NC_000014.7:g.60181277C= NCBI36
NG_008231.1:g.9632G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*1477G= MANE Select ENSP00000494686.1:n.*1477G=
ENST00000247182.6:c.*1477G= ENSP00000247182.5:n.*1477G=
ENST00000554986.2:c.*1477G= ENSP00000452700.2:n.*1477G=
NM_005982.3:c.*1477G= NP_005973.1:n.*1477G=
XM_017021602.2:c.*1751G= XP_016877091.1:n.*1751G=
NM_005982.4:c.*1477G= MANE Select NP_005973.1:n.*1477G=