Canonical Allele Identifier: CA1777410469
Gene: STAR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145529C= , CM000670.2:g.38145529C= GRCh38
NC_000008.10:g.38003047C= , CM000670.1:g.38003047C= GRCh37
NC_000008.9:g.38122204C= NCBI36
NG_011827.1:g.10554G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.651-214G= MANE Select ENSP00000276449.3:n.651-214G=
ENST00000276449.8:c.651-214G= ENSP00000276449.3:n.651-214G=
ENST00000520114.1:n.1571G=
ENST00000522050.1:c.586+434G=
NM_000349.2:c.651-214G= NP_000340.2:n.651-214G=
XM_006716392.1:c.650+434G= XP_006716455.1:n.650+434G=
NM_000349.3:c.651-214G= MANE Select NP_000340.2:n.651-214G=
Search 100 bp 5'
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