Canonical Allele Identifier: CA581110006
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1223783938
gnomAD v2: 8-38003175-AT-A
gnomAD v3: 8-38145657-AT-A
gnomAD v4: 8-38145657-AT-A
MyVariant Identifiers: chr8:g.38003176del (hg19) chr8:g.38145658del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145661del , CM000670.2:g.38145661del GRCh38
NC_000008.10:g.38003179del , CM000670.1:g.38003179del GRCh37
NC_000008.9:g.38122336del NCBI36
NG_011827.1:g.10425del

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.650+305del MANE Select ENSP00000276449.3:n.650+305del
ENST00000276449.8:c.650+305del ENSP00000276449.3:n.650+305del
ENST00000520114.1:n.1442del
ENST00000522050.1:c.586+305del
NM_000349.2:c.650+305del NP_000340.2:n.650+305del
XM_006716392.1:c.650+305del XP_006716455.1:n.650+305del
NM_000349.3:c.650+305del MANE Select NP_000340.2:n.650+305del
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Search 100 bp 3'