Canonical Allele Identifier: CA2140882720
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649621_60649622delinsCG , CM000676.2:g.60649621_60649622delinsCG GRCh38
NC_000014.8:g.61116339_61116340delinsCG , CM000676.1:g.61116339_61116340delinsCG GRCh37
NC_000014.7:g.60186092_60186093delinsCG NCBI36
NG_008231.1:g.4816_4817delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2313_248+2314delinsCG
ENST00000554986.2:c.42-3045_42-3044delinsCG ENSP00000452700.2:n.42-3045_42-3044delinsCG
ENST00000555955.3:n.1197+2313_1197+2314delinsCG