Canonical Allele Identifier: CA370698899

Gene: STAR

Linked Data

• MyVariant Identifiers: chr8:g.38003515A>T (hg19) ; chr8:g.38145997A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38145997A>T , CM000670.2:g.38145997A>T	GRCh38
NC_000008.10:g.38003515A>T , CM000670.1:g.38003515A>T	GRCh37
NC_000008.9:g.38122672A>T	NCBI36
NG_011827.1:g.10086T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.616T>A MANE Select	ENSP00000276449.3:p.Phe206Ile
ENST00000276449.8:c.616T>A	ENSP00000276449.3:p.Phe206Ile
ENST00000520114.1:n.1103T>A
ENST00000522050.1:c.552T>A
NM_000349.2:c.616T>A	NP_000340.2:p.Phe206Ile
XM_006716392.1:c.616T>A	XP_006716455.1:p.Phe206Ile
NM_000349.3:c.616T>A MANE Select	NP_000340.2:p.Phe206Ile