Canonical Allele Identifier: CA1777410538
Gene: STAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145636_38145639delinsAGTG , CM000670.2:g.38145636_38145639delinsAGTG GRCh38
NC_000008.10:g.38003154_38003157delinsAGTG , CM000670.1:g.38003154_38003157delinsAGTG GRCh37
NC_000008.9:g.38122311_38122314delinsAGTG NCBI36
NG_011827.1:g.10444_10447delinsCACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.651-324_651-321delinsCACT MANE Select ENSP00000276449.3:n.651-324_651-321delinsCACT
ENST00000276449.8:c.651-324_651-321delinsCACT ENSP00000276449.3:n.651-324_651-321delinsCACT
ENST00000520114.1:n.1461_1464delinsCACT
ENST00000522050.1:c.586+324_586+327delinsCACT
NM_000349.2:c.651-324_651-321delinsCACT NP_000340.2:n.651-324_651-321delinsCACT
XM_006716392.1:c.650+324_650+327delinsCACT XP_006716455.1:n.650+324_650+327delinsCACT
NM_000349.3:c.651-324_651-321delinsCACT MANE Select NP_000340.2:n.651-324_651-321delinsCACT