Canonical Allele Identifier: CA1777413579
Gene: STAR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38148628C= , CM000670.2:g.38148628C= GRCh38
NC_000008.10:g.38006146C= , CM000670.1:g.38006146C= GRCh37
NC_000008.9:g.38125303C= NCBI36
NG_011827.1:g.7455G=

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.178+13G= MANE Select ENSP00000276449.3:n.178+13G=
ENST00000276449.8:c.178+13G= ENSP00000276449.3:n.178+13G=
ENST00000520114.1:n.365G=
ENST00000521236.1:c.-101+13G= ENSP00000430030.1:n.-101+13G=
ENST00000522050.1:c.114+13G=
NM_000349.2:c.178+13G= NP_000340.2:n.178+13G=
XM_006716392.1:c.178+13G= XP_006716455.1:n.178+13G=
NM_000349.3:c.178+13G= MANE Select NP_000340.2:n.178+13G=
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