Canonical Allele Identifier: CA2338594241
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766404T= , CM000681.2:g.45766404T= GRCh38
NC_000019.9:g.46269662T= , CM000681.1:g.46269662T= GRCh37
NC_000019.8:g.50961502T= NCBI36
NG_012745.1:g.7836A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1555A= MANE Select ENSP00000316842.4:p.Ile519=
ENST00000317578.6:c.1555A= ENSP00000316842.4:p.Ile519=
ENST00000560160.1:c.587-293A=
ENST00000560168.1:c.*743A= ENSP00000453189.2:n.*743A=
ENST00000622857.1:c.16-442A= ENSP00000481365.1:n.16-442A=
NM_175875.4:c.1555A= NP_787071.2:p.Ile519=
NM_175875.5:c.1555A= MANE Select NP_787071.3:p.Ile519=