Canonical Allele Identifier: CA2140882199
Gene: SIX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649464T= , CM000676.2:g.60649464T= GRCh38
NC_000014.8:g.61116182T= , CM000676.1:g.61116182T= GRCh37
NC_000014.7:g.60185935T= NCBI36
NG_008231.1:g.4974A=

Transcript Alleles

HGVS Amino-acid change
ENST00000645694.3:c.-275A= MANE Select ENSP00000494686.1:n.-275A=
ENST00000553535.2:n.248+2471A=
ENST00000554986.2:c.42-2887A= ENSP00000452700.2:n.42-2887A=
ENST00000555955.3:n.1197+2471A=
XM_017021602.2:c.-275A= XP_016877091.1:n.-275A=
NM_005982.4:c.-275A= MANE Select NP_005973.1:n.-275A=