Canonical Allele Identifier: CA406419645
Gene: SIX5 HGNC NCBI

Linked Data

dbSNP Id: rs1223457785

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766887G>A , CM000681.2:g.45766887G>A GRCh38
NC_000019.9:g.46270145G>A , CM000681.1:g.46270145G>A GRCh37
NC_000019.8:g.50961985G>A NCBI36
NG_012745.1:g.7353C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1072C>T MANE Select ENSP00000316842.4:p.Pro358Ser
ENST00000317578.6:c.1072C>T ENSP00000316842.4:p.Pro358Ser
ENST00000560160.1:c.587-776C>T
ENST00000560168.1:c.*260C>T ENSP00000453189.2:n.*260C>T
ENST00000622857.1:c.16-925C>T ENSP00000481365.1:n.16-925C>T
NM_175875.4:c.1072C>T NP_787071.2:p.Pro358Ser
NM_175875.5:c.1072C>T MANE Select NP_787071.3:p.Pro358Ser