Canonical Allele Identifier: CA1777411299
Gene: STAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146266A= , CM000670.2:g.38146266A= GRCh38
NC_000008.10:g.38003784A= , CM000670.1:g.38003784A= GRCh37
NC_000008.9:g.38122941A= NCBI36
NG_011827.1:g.9817T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.465+23T= MANE Select ENSP00000276449.3:n.465+23T=
ENST00000276449.8:c.465+23T= ENSP00000276449.3:n.465+23T=
ENST00000520114.1:n.952+23T=
ENST00000522050.1:c.401+23T=
NM_000349.2:c.465+23T= NP_000340.2:n.465+23T=
XM_006716392.1:c.465+23T= XP_006716455.1:n.465+23T=
NM_000349.3:c.465+23T= MANE Select NP_000340.2:n.465+23T=