Canonical Allele Identifier: CA2140896808

Gene: SIX1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60644683_60644687delinsACAAG , CM000676.2:g.60644683_60644687delinsACAAG	GRCh38
NC_000014.8:g.61111401_61111405delinsACAAG , CM000676.1:g.61111401_61111405delinsACAAG	GRCh37
NC_000014.7:g.60181154_60181158delinsACAAG	NCBI36
NG_008231.1:g.9751_9755delinsCTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645694.3:c.*1596_*1600delinsCTTGT MANE Select	ENSP00000494686.1:n.*1596_*1600delinsCTTGT
ENST00000247182.6:c.*1596_*1600delinsCTTGT	ENSP00000247182.5:n.*1596_*1600delinsCTTGT
NM_005982.4:c.*1596_*1600delinsCTTGT MANE Select	NP_005973.1:n.*1596_*1600delinsCTTGT