Canonical Allele Identifier: CA406419507
Gene: SIX5 HGNC NCBI

Linked Data

dbSNP Id: rs201391763

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766854G>A , CM000681.2:g.45766854G>A GRCh38
NC_000019.9:g.46270112G>A , CM000681.1:g.46270112G>A GRCh37
NC_000019.8:g.50961952G>A NCBI36
NG_012745.1:g.7386C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1105C>T MANE Select ENSP00000316842.4:p.Pro369Ser
ENST00000317578.6:c.1105C>T ENSP00000316842.4:p.Pro369Ser
ENST00000560160.1:c.587-743C>T
ENST00000560168.1:c.*293C>T ENSP00000453189.2:n.*293C>T
ENST00000622857.1:c.16-892C>T ENSP00000481365.1:n.16-892C>T
NM_175875.4:c.1105C>T NP_787071.2:p.Pro369Ser
NM_175875.5:c.1105C>T MANE Select NP_787071.3:p.Pro369Ser