Canonical Allele Identifier: CA1777410487
Gene: STAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145581T= , CM000670.2:g.38145581T= GRCh38
NC_000008.10:g.38003099T= , CM000670.1:g.38003099T= GRCh37
NC_000008.9:g.38122256T= NCBI36
NG_011827.1:g.10502A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.651-266A= MANE Select ENSP00000276449.3:n.651-266A=
ENST00000276449.8:c.651-266A= ENSP00000276449.3:n.651-266A=
ENST00000520114.1:n.1519A=
ENST00000522050.1:c.586+382A=
NM_000349.2:c.651-266A= NP_000340.2:n.651-266A=
XM_006716392.1:c.650+382A= XP_006716455.1:n.650+382A=
NM_000349.3:c.651-266A= MANE Select NP_000340.2:n.651-266A=