Canonical Allele Identifier: CA2140882511
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649553_60649554delinsTC , CM000676.2:g.60649553_60649554delinsTC GRCh38
NC_000014.8:g.61116271_61116272delinsTC , CM000676.1:g.61116271_61116272delinsTC GRCh37
NC_000014.7:g.60186024_60186025delinsTC NCBI36
NG_008231.1:g.4884_4885delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2381_248+2382delinsGA
ENST00000554986.2:c.42-2977_42-2976delinsGA ENSP00000452700.2:n.42-2977_42-2976delinsGA
ENST00000555955.3:n.1197+2381_1197+2382delinsGA