Canonical Allele Identifier: CA2140882212
Gene: SIX1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649468C= , CM000676.2:g.60649468C= GRCh38
NC_000014.8:g.61116186C= , CM000676.1:g.61116186C= GRCh37
NC_000014.7:g.60185939C= NCBI36
NG_008231.1:g.4970G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.-279G= MANE Select ENSP00000494686.1:n.-279G=
ENST00000553535.2:n.248+2467G=
ENST00000554986.2:c.42-2891G= ENSP00000452700.2:n.42-2891G=
ENST00000555955.3:n.1197+2467G=
XM_017021602.2:c.-279G= XP_016877091.1:n.-279G=
NM_005982.4:c.-279G= MANE Select NP_005973.1:n.-279G=
Search 100 bp 5'
Search 100 bp 3'