Canonical Allele Identifier: CA2338594335
Gene: SIX5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766579C= , CM000681.2:g.45766579C= GRCh38
NC_000019.9:g.46269837C= , CM000681.1:g.46269837C= GRCh37
NC_000019.8:g.50961677C= NCBI36
NG_012745.1:g.7661G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1380G= MANE Select ENSP00000316842.4:p.Pro460=
ENST00000317578.6:c.1380G= ENSP00000316842.4:p.Pro460=
ENST00000560160.1:c.587-468G=
ENST00000560168.1:c.*568G= ENSP00000453189.2:n.*568G=
ENST00000622857.1:c.16-617G= ENSP00000481365.1:n.16-617G=
NM_175875.4:c.1380G= NP_787071.2:p.Pro460=
NM_175875.5:c.1380G= MANE Select NP_787071.3:p.Pro460=
Search 100 bp 5'
Search 100 bp 3'