Canonical Allele Identifier: CA2140881699
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649327A= , CM000676.2:g.60649327A= GRCh38
NC_000014.8:g.61116045A= , CM000676.1:g.61116045A= GRCh37
NC_000014.7:g.60185798A= NCBI36
NG_008231.1:g.5111T=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.-138T= MANE Select ENSP00000494686.1:n.-138T=
ENST00000247182.6:c.-138T= ENSP00000247182.5:n.-138T=
ENST00000553535.2:n.248+2608T=
ENST00000554986.2:c.42-2750T= ENSP00000452700.2:n.42-2750T=
ENST00000555955.3:n.1197+2608T=
NM_005982.3:c.-138T= NP_005973.1:n.-138T=
XM_017021602.2:c.-138T= XP_016877091.1:n.-138T=
NM_005982.4:c.-138T= MANE Select NP_005973.1:n.-138T=