Canonical Allele Identifier: CA2338594332
Gene: SIX5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766576C= , CM000681.2:g.45766576C= GRCh38
NC_000019.9:g.46269834C= , CM000681.1:g.46269834C= GRCh37
NC_000019.8:g.50961674C= NCBI36
NG_012745.1:g.7664G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1383G= MANE Select ENSP00000316842.4:p.Gly461=
ENST00000317578.6:c.1383G= ENSP00000316842.4:p.Gly461=
ENST00000560160.1:c.587-465G=
ENST00000560168.1:c.*571G= ENSP00000453189.2:n.*571G=
ENST00000622857.1:c.16-614G= ENSP00000481365.1:n.16-614G=
NM_175875.4:c.1383G= NP_787071.2:p.Gly461=
NM_175875.5:c.1383G= MANE Select NP_787071.3:p.Gly461=
Search 100 bp 5'
Search 100 bp 3'