Canonical Allele Identifier: CA370699479

Gene: STAR

Linked Data

• MyVariant Identifiers: chr8:g.38003605C>T (hg19) ; chr8:g.38146087C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38146087C>T , CM000670.2:g.38146087C>T	GRCh38
NC_000008.10:g.38003605C>T , CM000670.1:g.38003605C>T	GRCh37
NC_000008.9:g.38122762C>T	NCBI36
NG_011827.1:g.9996G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.526G>A MANE Select	ENSP00000276449.3:p.Gly176Arg
ENST00000276449.8:c.526G>A	ENSP00000276449.3:p.Gly176Arg
ENST00000520114.1:n.1013G>A
ENST00000522050.1:c.462G>A
NM_000349.2:c.526G>A	NP_000340.2:p.Gly176Arg
XM_006716392.1:c.526G>A	XP_006716455.1:p.Gly176Arg
NM_000349.3:c.526G>A MANE Select	NP_000340.2:p.Gly176Arg