Canonical Allele Identifier: CA2140896851

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60644746A= , CM000676.2:g.60644746A=	GRCh38
NC_000014.8:g.61111464A= , CM000676.1:g.61111464A=	GRCh37
NC_000014.7:g.60181217A=	NCBI36
NG_008231.1:g.9692T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645694.3:c.*1537T= MANE Select	ENSP00000494686.1:n.*1537T=
ENST00000247182.6:c.*1537T=	ENSP00000247182.5:n.*1537T=
ENST00000554986.2:c.*1537T=	ENSP00000452700.2:n.*1537T=
NM_005982.3:c.*1537T=	NP_005973.1:n.*1537T=
XM_017021602.2:c.*1811T=	XP_016877091.1:n.*1811T=
NM_005982.4:c.*1537T= MANE Select	NP_005973.1:n.*1537T=