Canonical Allele Identifier: CA851448769

Gene: STAR

Linked Data

• dbSNP Id: rs1226904173
• MyVariant Identifiers: chr8:g.38004503_38004516del (hg19) ; chr8:g.38146985_38146998del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38146992_38147005del , CM000670.2:g.38146992_38147005del	GRCh38
NC_000008.10:g.38004510_38004523del , CM000670.1:g.38004510_38004523del	GRCh37
NC_000008.9:g.38123667_38123680del	NCBI36
NG_011827.1:g.9085_9098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.307-551_307-538del MANE Select	ENSP00000276449.3:n.307-551_307-538del
ENST00000276449.8:c.307-551_307-538del	ENSP00000276449.3:n.307-551_307-538del
ENST00000520114.1:n.794-551_794-538del
ENST00000521236.1:c.61-551_61-538del	ENSP00000430030.1:n.61-551_61-538del
ENST00000522050.1:c.243-551_243-538del
NM_000349.2:c.307-551_307-538del	NP_000340.2:n.307-551_307-538del
XM_006716392.1:c.307-551_307-538del	XP_006716455.1:n.307-551_307-538del
NM_000349.3:c.307-551_307-538del MANE Select	NP_000340.2:n.307-551_307-538del