Canonical Allele Identifier: CA1777410788
Gene: STAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38145920_38145922delinsCTG , CM000670.2:g.38145920_38145922delinsCTG GRCh38
NC_000008.10:g.38003438_38003440delinsCTG , CM000670.1:g.38003438_38003440delinsCTG GRCh37
NC_000008.9:g.38122595_38122597delinsCTG NCBI36
NG_011827.1:g.10161_10163delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000276449.9:c.650+41_650+43delinsCAG MANE Select ENSP00000276449.3:n.650+41_650+43delinsCAG
ENST00000276449.8:c.650+41_650+43delinsCAG ENSP00000276449.3:n.650+41_650+43delinsCAG
ENST00000520114.1:n.1178_1180delinsCAG
ENST00000522050.1:c.586+41_586+43delinsCAG
NM_000349.2:c.650+41_650+43delinsCAG NP_000340.2:n.650+41_650+43delinsCAG
XM_006716392.1:c.650+41_650+43delinsCAG XP_006716455.1:n.650+41_650+43delinsCAG
NM_000349.3:c.650+41_650+43delinsCAG MANE Select NP_000340.2:n.650+41_650+43delinsCAG