Canonical Allele Identifier: CA460374938

Gene: STAR

Linked Data

• MyVariant Identifiers: chr8:g.38001836C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38144318C>A , CM000670.2:g.38144318C>A	GRCh38
NC_000008.10:g.38001836C>A , CM000670.1:g.38001836C>A	GRCh37
NC_000008.9:g.38120993C>A	NCBI36
NG_011827.1:g.11765G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.813G>T MANE Select	ENSP00000276449.3:p.Leu271=
ENST00000276449.8:c.813G>T	ENSP00000276449.3:p.Leu271=
ENST00000520114.1:n.2782G>T
ENST00000522050.1:c.655G>T
NM_000349.2:c.813G>T	NP_000340.2:p.Leu271=
XM_006716392.1:c.719G>T	XP_006716455.1:p.Cys240Phe
NM_000349.3:c.813G>T MANE Select	NP_000340.2:p.Leu271=