Canonical Allele Identifier: CA2140879414

Gene: SIX1 MIR9718

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60648706C= , CM000676.2:g.60648706C=	GRCh38
NC_000014.8:g.61115424C= , CM000676.1:g.61115424C=	GRCh37
NC_000014.7:g.60185177C=	NCBI36
NG_008231.1:g.5732G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000645694.3:c.484G= (SIX1) MANE Select	ENSP00000494686.1:p.Gly162=
ENST00000247182.6:c.484G= (SIX1)	ENSP00000247182.5:p.Gly162=
ENST00000553535.2:n.249-2129G= (SIX1)
ENST00000554986.2:c.42-2129G= (SIX1)	ENSP00000452700.2:n.42-2129G=
ENST00000555955.3:n.1198-2129G= (SIX1)
NM_005982.3:c.484G= (SIX1)	NP_005973.1:p.Gly162=
XM_017021602.2:c.484G= (SIX1)	XP_016877091.1:p.Gly162=
NM_005982.4:c.484G= (SIX1) MANE Select	NP_005973.1:p.Gly162=
NR_162089.1:n.59C= (MIR9718)