Canonical Allele Identifier: CA2140897079
Gene: SIX1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645040A= , CM000676.2:g.60645040A= GRCh38
NC_000014.8:g.61111758A= , CM000676.1:g.61111758A= GRCh37
NC_000014.7:g.60181511A= NCBI36
NG_008231.1:g.9398T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*1243T= MANE Select ENSP00000494686.1:n.*1243T=
ENST00000247182.6:c.*1243T= ENSP00000247182.5:n.*1243T=
ENST00000554986.2:c.*1243T= ENSP00000452700.2:n.*1243T=
ENST00000555955.3:n.2735T=
NM_005982.3:c.*1243T= NP_005973.1:n.*1243T=
XM_017021602.2:c.*1517T= XP_016877091.1:n.*1517T=
NM_005982.4:c.*1243T= MANE Select NP_005973.1:n.*1243T=
Search 100 bp 5'
Search 100 bp 3'