Canonical Allele Identifier: CA1777411966

Gene: STAR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38146879_38146890delinsGCCTGGAACTGT , CM000670.2:g.38146879_38146890delinsGCCTGGAACTGT	GRCh38
NC_000008.10:g.38004397_38004408delinsGCCTGGAACTGT , CM000670.1:g.38004397_38004408delinsGCCTGGAACTGT	GRCh37
NC_000008.9:g.38123554_38123565delinsGCCTGGAACTGT	NCBI36
NG_011827.1:g.9193_9204delinsACAGTTCCAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.307-443_307-432delinsACAGTTCCAGGC MANE Select	ENSP00000276449.3:n.307-443_307-432delinsACAGTTCCAGGC
ENST00000276449.8:c.307-443_307-432delinsACAGTTCCAGGC	ENSP00000276449.3:n.307-443_307-432delinsACAGTTCCAGGC
ENST00000520114.1:n.794-443_794-432delinsACAGTTCCAGGC
ENST00000521236.1:c.61-443_61-432delinsACAGTTCCAGGC	ENSP00000430030.1:n.61-443_61-432delinsACAGTTCCAGGC
ENST00000522050.1:c.243-443_243-432delinsACAGTTCCAGGC
NM_000349.2:c.307-443_307-432delinsACAGTTCCAGGC	NP_000340.2:n.307-443_307-432delinsACAGTTCCAGGC
XM_006716392.1:c.307-443_307-432delinsACAGTTCCAGGC	XP_006716455.1:n.307-443_307-432delinsACAGTTCCAGGC
NM_000349.3:c.307-443_307-432delinsACAGTTCCAGGC MANE Select	NP_000340.2:n.307-443_307-432delinsACAGTTCCAGGC