Canonical Allele Identifier: CA175096464
Gene: STAR HGNC NCBI

Linked Data

dbSNP Id: rs1044977533
gnomAD v2: 8-38004416-T-TA
gnomAD v3: 8-38146898-T-TA
gnomAD v4: 8-38146898-T-TA
MyVariant Identifiers: chr8:g.38004416_38004417insA (hg19) chr8:g.38146898_38146899insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146899dup , CM000670.2:g.38146899dup GRCh38
NC_000008.10:g.38004417dup , CM000670.1:g.38004417dup GRCh37
NC_000008.9:g.38123574dup NCBI36
NG_011827.1:g.9184dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.307-452dup MANE Select ENSP00000276449.3:n.307-452dup
ENST00000276449.8:c.307-452dup ENSP00000276449.3:n.307-452dup
ENST00000520114.1:n.794-452dup
ENST00000521236.1:c.61-452dup ENSP00000430030.1:n.61-452dup
ENST00000522050.1:c.243-452dup
NM_000349.2:c.307-452dup NP_000340.2:n.307-452dup
XM_006716392.1:c.307-452dup XP_006716455.1:n.307-452dup
NM_000349.3:c.307-452dup MANE Select NP_000340.2:n.307-452dup
Search 100 bp 5'
Search 100 bp 3'