Canonical Allele Identifier: CA2338594482
Gene: SIX5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766814G= , CM000681.2:g.45766814G= GRCh38
NC_000019.9:g.46270072G= , CM000681.1:g.46270072G= GRCh37
NC_000019.8:g.50961912G= NCBI36
NG_012745.1:g.7426C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1145C= MANE Select ENSP00000316842.4:p.Thr382=
ENST00000317578.6:c.1145C= ENSP00000316842.4:p.Thr382=
ENST00000560160.1:c.587-703C=
ENST00000560168.1:c.*333C= ENSP00000453189.2:n.*333C=
ENST00000622857.1:c.16-852C= ENSP00000481365.1:n.16-852C=
NM_175875.4:c.1145C= NP_787071.2:p.Thr382=
NM_175875.5:c.1145C= MANE Select NP_787071.3:p.Thr382=
Search 100 bp 5'
Search 100 bp 3'