Canonical Allele Identifier: CA2140896894
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60644788G= , CM000676.2:g.60644788G= GRCh38
NC_000014.8:g.61111506G= , CM000676.1:g.61111506G= GRCh37
NC_000014.7:g.60181259G= NCBI36
NG_008231.1:g.9650C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*1495C= MANE Select ENSP00000494686.1:n.*1495C=
ENST00000247182.6:c.*1495C= ENSP00000247182.5:n.*1495C=
ENST00000554986.2:c.*1495C= ENSP00000452700.2:n.*1495C=
NM_005982.3:c.*1495C= NP_005973.1:n.*1495C=
XM_017021602.2:c.*1769C= XP_016877091.1:n.*1769C=
NM_005982.4:c.*1495C= MANE Select NP_005973.1:n.*1495C=