Canonical Allele Identifier: CA460496891

Gene: STAR

Linked Data

• MyVariant Identifiers: chr8:g.38003543G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38146025G>T , CM000670.2:g.38146025G>T	GRCh38
NC_000008.10:g.38003543G>T , CM000670.1:g.38003543G>T	GRCh37
NC_000008.9:g.38122700G>T	NCBI36
NG_011827.1:g.10058C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.588C>A MANE Select	ENSP00000276449.3:p.Thr196=
ENST00000276449.8:c.588C>A	ENSP00000276449.3:p.Thr196=
ENST00000520114.1:n.1075C>A
ENST00000522050.1:c.524C>A
NM_000349.2:c.588C>A	NP_000340.2:p.Thr196=
XM_006716392.1:c.588C>A	XP_006716455.1:p.Thr196=
NM_000349.3:c.588C>A MANE Select	NP_000340.2:p.Thr196=