Canonical Allele Identifier: CA1777411990
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1802583914

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146901_38146902del , CM000670.2:g.38146901_38146902del GRCh38
NC_000008.10:g.38004419_38004420del , CM000670.1:g.38004419_38004420del GRCh37
NC_000008.9:g.38123576_38123577del NCBI36
NG_011827.1:g.9183_9184del

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.307-453_307-452del MANE Select ENSP00000276449.3:n.307-453_307-452del
ENST00000276449.8:c.307-453_307-452del ENSP00000276449.3:n.307-453_307-452del
ENST00000520114.1:n.794-453_794-452del
ENST00000521236.1:c.61-453_61-452del ENSP00000430030.1:n.61-453_61-452del
ENST00000522050.1:c.243-453_243-452del
NM_000349.2:c.307-453_307-452del NP_000340.2:n.307-453_307-452del
XM_006716392.1:c.307-453_307-452del XP_006716455.1:n.307-453_307-452del
NM_000349.3:c.307-453_307-452del MANE Select NP_000340.2:n.307-453_307-452del