Canonical Allele Identifier: CA2140897351
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645431T= , CM000676.2:g.60645431T= GRCh38
NC_000014.8:g.61112149T= , CM000676.1:g.61112149T= GRCh37
NC_000014.7:g.60181902T= NCBI36
NG_008231.1:g.9007A=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.*852A= MANE Select ENSP00000494686.1:n.*852A=
ENST00000247182.6:c.*852A= ENSP00000247182.5:n.*852A=
ENST00000553535.2:n.1395A=
ENST00000554986.2:c.*852A= ENSP00000452700.2:n.*852A=
ENST00000555955.3:n.2344A=
NM_005982.3:c.*852A= NP_005973.1:n.*852A=
XM_017021602.2:c.*1126A= XP_016877091.1:n.*1126A=
NM_005982.4:c.*852A= MANE Select NP_005973.1:n.*852A=