Canonical Allele Identifier: CA2338594574
Gene: SIX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766972T= , CM000681.2:g.45766972T= GRCh38
NC_000019.9:g.46270230T= , CM000681.1:g.46270230T= GRCh37
NC_000019.8:g.50962070T= NCBI36
NG_012745.1:g.7268A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.987A= MANE Select ENSP00000316842.4:p.Ala329=
ENST00000317578.6:c.987A= ENSP00000316842.4:p.Ala329=
ENST00000560160.1:c.587-861A=
ENST00000560168.1:c.*175A= ENSP00000453189.2:n.*175A=
ENST00000622857.1:c.16-1010A= ENSP00000481365.1:n.16-1010A=
NM_175875.4:c.987A= NP_787071.2:p.Ala329=
NM_175875.5:c.987A= MANE Select NP_787071.3:p.Ala329=