Canonical Allele Identifier: CA2140882697
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649617_60649618delinsAG , CM000676.2:g.60649617_60649618delinsAG GRCh38
NC_000014.8:g.61116335_61116336delinsAG , CM000676.1:g.61116335_61116336delinsAG GRCh37
NC_000014.7:g.60186088_60186089delinsAG NCBI36
NG_008231.1:g.4820_4821delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000553535.2:n.248+2317_248+2318delinsCT
ENST00000554986.2:c.42-3041_42-3040delinsCT ENSP00000452700.2:n.42-3041_42-3040delinsCT
ENST00000555955.3:n.1197+2317_1197+2318delinsCT