Canonical Allele Identifier: CA2140881244

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60649209_60649210delinsGC , CM000676.2:g.60649209_60649210delinsGC	GRCh38
NC_000014.8:g.61115927_61115928delinsGC , CM000676.1:g.61115927_61115928delinsGC	GRCh37
NC_000014.7:g.60185680_60185681delinsGC	NCBI36
NG_008231.1:g.5228_5229delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645694.3:c.-21_-20delinsGC MANE Select	ENSP00000494686.1:n.-21_-20delinsGC
ENST00000247182.6:c.-21_-20delinsGC	ENSP00000247182.5:n.-21_-20delinsGC
ENST00000553535.2:n.249-2633_249-2632delinsGC
ENST00000554986.2:c.42-2633_42-2632delinsGC	ENSP00000452700.2:n.42-2633_42-2632delinsGC
ENST00000555955.3:n.1198-2633_1198-2632delinsGC
NM_005982.3:c.-21_-20delinsGC	NP_005973.1:n.-21_-20delinsGC
XM_017021602.2:c.-21_-20delinsGC	XP_016877091.1:n.-21_-20delinsGC
NM_005982.4:c.-21_-20delinsGC MANE Select	NP_005973.1:n.-21_-20delinsGC