Canonical Allele Identifier: CA2140896870

Gene: SIX1

Linked Data

• dbSNP Id: rs1894911515

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60644765del , CM000676.2:g.60644765del	GRCh38
NC_000014.8:g.61111483del , CM000676.1:g.61111483del	GRCh37
NC_000014.7:g.60181236del	NCBI36
NG_008231.1:g.9673del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645694.3:c.*1518del MANE Select	ENSP00000494686.1:n.*1518del
ENST00000247182.6:c.*1518del	ENSP00000247182.5:n.*1518del
ENST00000554986.2:c.*1518del	ENSP00000452700.2:n.*1518del
NM_005982.3:c.*1518del	NP_005973.1:n.*1518del
XM_017021602.2:c.*1792del	XP_016877091.1:n.*1792del
NM_005982.4:c.*1518del MANE Select	NP_005973.1:n.*1518del