Canonical Allele Identifier: CA2140881640

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60649309_60649310delinsTG , CM000676.2:g.60649309_60649310delinsTG	GRCh38
NC_000014.8:g.61116027_61116028delinsTG , CM000676.1:g.61116027_61116028delinsTG	GRCh37
NC_000014.7:g.60185780_60185781delinsTG	NCBI36
NG_008231.1:g.5128_5129delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000645694.3:c.-121_-120delinsCA MANE Select	ENSP00000494686.1:n.-121_-120delinsCA
ENST00000247182.6:c.-121_-120delinsCA	ENSP00000247182.5:n.-121_-120delinsCA
ENST00000553535.2:n.248+2625_248+2626delinsCA
ENST00000554986.2:c.42-2733_42-2732delinsCA	ENSP00000452700.2:n.42-2733_42-2732delinsCA
ENST00000555955.3:n.1197+2625_1197+2626delinsCA
NM_005982.3:c.-121_-120delinsCA	NP_005973.1:n.-121_-120delinsCA
XM_017021602.2:c.-121_-120delinsCA	XP_016877091.1:n.-121_-120delinsCA
NM_005982.4:c.-121_-120delinsCA MANE Select	NP_005973.1:n.-121_-120delinsCA