Canonical Allele Identifier: CA406420879
Gene: SIX5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.46270272G>T (hg19) chr19:g.45767014G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45767014G>T , CM000681.2:g.45767014G>T GRCh38
NC_000019.9:g.46270272G>T , CM000681.1:g.46270272G>T GRCh37
NC_000019.8:g.50962112G>T NCBI36
NG_012745.1:g.7226C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.945C>A MANE Select ENSP00000316842.4:p.Cys315Ter
ENST00000317578.6:c.945C>A ENSP00000316842.4:p.Cys315Ter
ENST00000560160.1:c.587-903C>A
ENST00000560168.1:c.*133C>A ENSP00000453189.2:n.*133C>A
ENST00000622857.1:c.16-1052C>A ENSP00000481365.1:n.16-1052C>A
NM_175875.4:c.945C>A NP_787071.2:p.Cys315Ter
NM_175875.5:c.945C>A MANE Select NP_787071.3:p.Cys315Ter
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