Canonical Allele Identifier: CA2140897371

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60645466C= , CM000676.2:g.60645466C=	GRCh38
NC_000014.8:g.61112184C= , CM000676.1:g.61112184C=	GRCh37
NC_000014.7:g.60181937C=	NCBI36
NG_008231.1:g.8972G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000645694.3:c.*817G= MANE Select	ENSP00000494686.1:n.*817G=
ENST00000247182.6:c.*817G=	ENSP00000247182.5:n.*817G=
ENST00000553535.2:n.1360G=
ENST00000554986.2:c.*817G=	ENSP00000452700.2:n.*817G=
ENST00000555955.3:n.2309G=
NM_005982.3:c.*817G=	NP_005973.1:n.*817G=
XM_017021602.2:c.*1091G=	XP_016877091.1:n.*1091G=
NM_005982.4:c.*817G= MANE Select	NP_005973.1:n.*817G=