Canonical Allele Identifier: CA2140881696
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649326G= , CM000676.2:g.60649326G= GRCh38
NC_000014.8:g.61116044G= , CM000676.1:g.61116044G= GRCh37
NC_000014.7:g.60185797G= NCBI36
NG_008231.1:g.5112C=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.-137C= MANE Select ENSP00000494686.1:n.-137C=
ENST00000247182.6:c.-137C= ENSP00000247182.5:n.-137C=
ENST00000553535.2:n.248+2609C=
ENST00000554986.2:c.42-2749C= ENSP00000452700.2:n.42-2749C=
ENST00000555955.3:n.1197+2609C=
NM_005982.3:c.-137C= NP_005973.1:n.-137C=
XM_017021602.2:c.-137C= XP_016877091.1:n.-137C=
NM_005982.4:c.-137C= MANE Select NP_005973.1:n.-137C=