Canonical Allele Identifier: CA851448765
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1270449019
gnomAD v3: 8-38146984-A-AT
gnomAD v4: 8-38146984-A-AT
MyVariant Identifiers: chr8:g.38004502_38004503insT (hg19) chr8:g.38146984_38146985insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146991dup , CM000670.2:g.38146991dup GRCh38
NC_000008.10:g.38004509dup , CM000670.1:g.38004509dup GRCh37
NC_000008.9:g.38123666dup NCBI36
NG_011827.1:g.9098dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.307-538dup MANE Select ENSP00000276449.3:n.307-538dup
ENST00000276449.8:c.307-538dup ENSP00000276449.3:n.307-538dup
ENST00000520114.1:n.794-538dup
ENST00000521236.1:c.61-538dup ENSP00000430030.1:n.61-538dup
ENST00000522050.1:c.243-538dup
NM_000349.2:c.307-538dup NP_000340.2:n.307-538dup
XM_006716392.1:c.307-538dup XP_006716455.1:n.307-538dup
NM_000349.3:c.307-538dup MANE Select NP_000340.2:n.307-538dup
Search 100 bp 5'
Search 100 bp 3'