Canonical Allele Identifier: CA370696135

Gene: STAR

Linked Data

• MyVariant Identifiers: chr8:g.38001891T>G (hg19) ; chr8:g.38144373T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38144373T>G , CM000670.2:g.38144373T>G	GRCh38
NC_000008.10:g.38001891T>G , CM000670.1:g.38001891T>G	GRCh37
NC_000008.9:g.38121048T>G	NCBI36
NG_011827.1:g.11710A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.758A>C MANE Select	ENSP00000276449.3:p.Lys253Thr
ENST00000276449.8:c.758A>C	ENSP00000276449.3:p.Lys253Thr
ENST00000520114.1:n.2727A>C
ENST00000522050.1:c.600A>C
NM_000349.2:c.758A>C	NP_000340.2:p.Lys253Thr
XM_006716392.1:c.664A>C	XP_006716455.1:p.Arg222=
NM_000349.3:c.758A>C MANE Select	NP_000340.2:p.Lys253Thr