Canonical Allele Identifier: CA2686932462
Gene: STAR HGNC NCBI

Linked Data

gnomAD v4: 8-38145522-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145522G>T , CM000670.2:g.38145522G>T GRCh38
NC_000008.10:g.38003040G>T , CM000670.1:g.38003040G>T GRCh37
NC_000008.9:g.38122197G>T NCBI36
NG_011827.1:g.10561C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.651-207C>A MANE Select ENSP00000276449.3:n.651-207C>A
ENST00000276449.8:c.651-207C>A ENSP00000276449.3:n.651-207C>A
ENST00000520114.1:n.1578C>A
ENST00000522050.1:c.586+441C>A
NM_000349.2:c.651-207C>A NP_000340.2:n.651-207C>A
XM_006716392.1:c.650+441C>A XP_006716455.1:n.650+441C>A
NM_000349.3:c.651-207C>A MANE Select NP_000340.2:n.651-207C>A
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