Canonical Allele Identifier: CA370696677

Gene: STAR

Linked Data

• MyVariant Identifiers: chr8:g.38002751T>A (hg19) ; chr8:g.38145233T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38145233T>A , CM000670.2:g.38145233T>A	GRCh38
NC_000008.10:g.38002751T>A , CM000670.1:g.38002751T>A	GRCh37
NC_000008.9:g.38121908T>A	NCBI36
NG_011827.1:g.10850A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000276449.9:c.733A>T MANE Select	ENSP00000276449.3:p.Ile245Phe
ENST00000276449.8:c.733A>T	ENSP00000276449.3:p.Ile245Phe
ENST00000520114.1:n.1867A>T
ENST00000522050.1:c.586+730A>T
NM_000349.2:c.733A>T	NP_000340.2:p.Ile245Phe
XM_006716392.1:c.650+730A>T	XP_006716455.1:n.650+730A>T
NM_000349.3:c.733A>T MANE Select	NP_000340.2:p.Ile245Phe