Canonical Allele Identifier: CA2338594330
Gene: SIX5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766571G= , CM000681.2:g.45766571G= GRCh38
NC_000019.9:g.46269829G= , CM000681.1:g.46269829G= GRCh37
NC_000019.8:g.50961669G= NCBI36
NG_012745.1:g.7669C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1388C= MANE Select ENSP00000316842.4:p.Pro463=
ENST00000317578.6:c.1388C= ENSP00000316842.4:p.Pro463=
ENST00000560160.1:c.587-460C=
ENST00000560168.1:c.*576C= ENSP00000453189.2:n.*576C=
ENST00000622857.1:c.16-609C= ENSP00000481365.1:n.16-609C=
NM_175875.4:c.1388C= NP_787071.2:p.Pro463=
NM_175875.5:c.1388C= MANE Select NP_787071.3:p.Pro463=
Search 100 bp 5'
Search 100 bp 3'