Canonical Allele Identifier: CA2140881814
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649365C= , CM000676.2:g.60649365C= GRCh38
NC_000014.8:g.61116083C= , CM000676.1:g.61116083C= GRCh37
NC_000014.7:g.60185836C= NCBI36
NG_008231.1:g.5073G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.-176G= MANE Select ENSP00000494686.1:n.-176G=
ENST00000247182.6:c.-176G= ENSP00000247182.5:n.-176G=
ENST00000553535.2:n.248+2570G=
ENST00000554986.2:c.42-2788G= ENSP00000452700.2:n.42-2788G=
ENST00000555955.3:n.1197+2570G=
NM_005982.3:c.-176G= NP_005973.1:n.-176G=
XM_017021602.2:c.-176G= XP_016877091.1:n.-176G=
NM_005982.4:c.-176G= MANE Select NP_005973.1:n.-176G=