Canonical Allele Identifier: CA1112877922
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1397231231
gnomAD v3: 8-38146767-CAA-C
gnomAD v4: 8-38146767-CAA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146777_38146778del , CM000670.2:g.38146777_38146778del GRCh38
NC_000008.10:g.38004295_38004296del , CM000670.1:g.38004295_38004296del GRCh37
NC_000008.9:g.38123452_38123453del NCBI36
NG_011827.1:g.9314_9315del

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.307-322_307-321del MANE Select ENSP00000276449.3:n.307-322_307-321del
ENST00000276449.8:c.307-322_307-321del ENSP00000276449.3:n.307-322_307-321del
ENST00000520114.1:n.794-322_794-321del
ENST00000521236.1:c.61-322_61-321del ENSP00000430030.1:n.61-322_61-321del
ENST00000522050.1:c.243-322_243-321del
NM_000349.2:c.307-322_307-321del NP_000340.2:n.307-322_307-321del
XM_006716392.1:c.307-322_307-321del XP_006716455.1:n.307-322_307-321del
NM_000349.3:c.307-322_307-321del MANE Select NP_000340.2:n.307-322_307-321del
Search 100 bp 5'
Search 100 bp 3'