Canonical Allele Identifier: CA2140896809

Gene: SIX1

Linked Data

• dbSNP Id: rs1894910309

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60644689_60644692del , CM000676.2:g.60644689_60644692del	GRCh38
NC_000014.8:g.61111407_61111410del , CM000676.1:g.61111407_61111410del	GRCh37
NC_000014.7:g.60181160_60181163del	NCBI36
NG_008231.1:g.9751_9754del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645694.3:c.*1596_*1599del MANE Select	ENSP00000494686.1:n.*1596_*1599del
ENST00000247182.6:c.*1596_*1599del	ENSP00000247182.5:n.*1596_*1599del
NM_005982.4:c.*1596_*1599del MANE Select	NP_005973.1:n.*1596_*1599del