Canonical Allele Identifier: CA2140881145
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649188A= , CM000676.2:g.60649188A= GRCh38
NC_000014.8:g.61115906A= , CM000676.1:g.61115906A= GRCh37
NC_000014.7:g.60185659A= NCBI36
NG_008231.1:g.5250T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.2T= MANE Select ENSP00000494686.1:p.Met1=
ENST00000247182.6:c.2T= ENSP00000247182.5:p.Met1=
ENST00000553535.2:n.249-2611T=
ENST00000554986.2:c.42-2611T= ENSP00000452700.2:n.42-2611T=
ENST00000555955.3:n.1198-2611T=
NM_005982.3:c.2T= NP_005973.1:p.Met1=
XM_017021602.2:c.2T= XP_016877091.1:p.Met1=
NM_005982.4:c.2T= MANE Select NP_005973.1:p.Met1=