Canonical Allele Identifier: CA2140882190
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649463G= , CM000676.2:g.60649463G= GRCh38
NC_000014.8:g.61116181G= , CM000676.1:g.61116181G= GRCh37
NC_000014.7:g.60185934G= NCBI36
NG_008231.1:g.4975C=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.-274C= MANE Select ENSP00000494686.1:n.-274C=
ENST00000553535.2:n.248+2472C=
ENST00000554986.2:c.42-2886C= ENSP00000452700.2:n.42-2886C=
ENST00000555955.3:n.1197+2472C=
XM_017021602.2:c.-274C= XP_016877091.1:n.-274C=
NM_005982.4:c.-274C= MANE Select NP_005973.1:n.-274C=