Canonical Allele Identifier: CA2140881234
Gene: SIX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60649208C= , CM000676.2:g.60649208C= GRCh38
NC_000014.8:g.61115926C= , CM000676.1:g.61115926C= GRCh37
NC_000014.7:g.60185679C= NCBI36
NG_008231.1:g.5230G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.-19G= MANE Select ENSP00000494686.1:n.-19G=
ENST00000247182.6:c.-19G= ENSP00000247182.5:n.-19G=
ENST00000553535.2:n.249-2631G=
ENST00000554986.2:c.42-2631G= ENSP00000452700.2:n.42-2631G=
ENST00000555955.3:n.1198-2631G=
NM_005982.3:c.-19G= NP_005973.1:n.-19G=
XM_017021602.2:c.-19G= XP_016877091.1:n.-19G=
NM_005982.4:c.-19G= MANE Select NP_005973.1:n.-19G=
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