Canonical Allele Identifier: CA2140897381
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645479G= , CM000676.2:g.60645479G= GRCh38
NC_000014.8:g.61112197G= , CM000676.1:g.61112197G= GRCh37
NC_000014.7:g.60181950G= NCBI36
NG_008231.1:g.8959C=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.*804C= MANE Select ENSP00000494686.1:n.*804C=
ENST00000247182.6:c.*804C= ENSP00000247182.5:n.*804C=
ENST00000553535.2:n.1347C=
ENST00000554986.2:c.*804C= ENSP00000452700.2:n.*804C=
ENST00000555955.3:n.2296C=
NM_005982.3:c.*804C= NP_005973.1:n.*804C=
XM_017021602.2:c.*1078C= XP_016877091.1:n.*1078C=
NM_005982.4:c.*804C= MANE Select NP_005973.1:n.*804C=