Canonical Allele Identifier: CA2140882181

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60649462A= , CM000676.2:g.60649462A=	GRCh38
NC_000014.8:g.61116180A= , CM000676.1:g.61116180A=	GRCh37
NC_000014.7:g.60185933A=	NCBI36
NG_008231.1:g.4976T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000645694.3:c.-273T= MANE Select	ENSP00000494686.1:n.-273T=
ENST00000247182.6:c.-273T=	ENSP00000247182.5:n.-273T=
ENST00000553535.2:n.248+2473T=
ENST00000554986.2:c.42-2885T=	ENSP00000452700.2:n.42-2885T=
ENST00000555955.3:n.1197+2473T=
XM_017021602.2:c.-273T=	XP_016877091.1:n.-273T=
NM_005982.4:c.-273T= MANE Select	NP_005973.1:n.-273T=