Canonical Allele Identifier: CA2338594522
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766881G= , CM000681.2:g.45766881G= GRCh38
NC_000019.9:g.46270139G= , CM000681.1:g.46270139G= GRCh37
NC_000019.8:g.50961979G= NCBI36
NG_012745.1:g.7359C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1078C= MANE Select ENSP00000316842.4:p.Leu360=
ENST00000317578.6:c.1078C= ENSP00000316842.4:p.Leu360=
ENST00000560160.1:c.587-770C=
ENST00000560168.1:c.*266C= ENSP00000453189.2:n.*266C=
ENST00000622857.1:c.16-919C= ENSP00000481365.1:n.16-919C=
NM_175875.4:c.1078C= NP_787071.2:p.Leu360=
NM_175875.5:c.1078C= MANE Select NP_787071.3:p.Leu360=