Canonical Allele Identifier: CA1777411287
Gene: STAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146239C= , CM000670.2:g.38146239C= GRCh38
NC_000008.10:g.38003757C= , CM000670.1:g.38003757C= GRCh37
NC_000008.9:g.38122914C= NCBI36
NG_011827.1:g.9844G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.465+50G= MANE Select ENSP00000276449.3:n.465+50G=
ENST00000276449.8:c.465+50G= ENSP00000276449.3:n.465+50G=
ENST00000520114.1:n.952+50G=
ENST00000522050.1:c.401+50G=
NM_000349.2:c.465+50G= NP_000340.2:n.465+50G=
XM_006716392.1:c.465+50G= XP_006716455.1:n.465+50G=
NM_000349.3:c.465+50G= MANE Select NP_000340.2:n.465+50G=