Canonical Allele Identifier: CA1777413488
Gene: STAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38148532T= , CM000670.2:g.38148532T= GRCh38
NC_000008.10:g.38006050T= , CM000670.1:g.38006050T= GRCh37
NC_000008.9:g.38125207T= NCBI36
NG_011827.1:g.7551A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.178+109A= MANE Select ENSP00000276449.3:n.178+109A=
ENST00000276449.8:c.178+109A= ENSP00000276449.3:n.178+109A=
ENST00000520114.1:n.461A=
ENST00000521236.1:c.-101+109A= ENSP00000430030.1:n.-101+109A=
ENST00000522050.1:c.114+109A=
NM_000349.2:c.178+109A= NP_000340.2:n.178+109A=
XM_006716392.1:c.178+109A= XP_006716455.1:n.178+109A=
NM_000349.3:c.178+109A= MANE Select NP_000340.2:n.178+109A=