Canonical Allele Identifier: CA2338594302
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766523A= , CM000681.2:g.45766523A= GRCh38
NC_000019.9:g.46269781A= , CM000681.1:g.46269781A= GRCh37
NC_000019.8:g.50961621A= NCBI36
NG_012745.1:g.7717T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1436T= MANE Select ENSP00000316842.4:p.Val479=
ENST00000317578.6:c.1436T= ENSP00000316842.4:p.Val479=
ENST00000560160.1:c.587-412T=
ENST00000560168.1:c.*624T= ENSP00000453189.2:n.*624T=
ENST00000622857.1:c.16-561T= ENSP00000481365.1:n.16-561T=
NM_175875.4:c.1436T= NP_787071.2:p.Val479=
NM_175875.5:c.1436T= MANE Select NP_787071.3:p.Val479=