Canonical Allele Identifier: CA2686932498

Gene: STAR

Linked Data

• gnomAD v4: 8-38145559-A-ACTG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38145560_38145562dup , CM000670.2:g.38145560_38145562dup	GRCh38
NC_000008.10:g.38003078_38003080dup , CM000670.1:g.38003078_38003080dup	GRCh37
NC_000008.9:g.38122235_38122237dup	NCBI36
NG_011827.1:g.10521_10523dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.651-247_651-245dup MANE Select	ENSP00000276449.3:n.651-247_651-245dup
ENST00000276449.8:c.651-247_651-245dup	ENSP00000276449.3:n.651-247_651-245dup
ENST00000520114.1:n.1538_1540dup
ENST00000522050.1:c.586+401_586+403dup
NM_000349.2:c.651-247_651-245dup	NP_000340.2:n.651-247_651-245dup
XM_006716392.1:c.650+401_650+403dup	XP_006716455.1:n.650+401_650+403dup
NM_000349.3:c.651-247_651-245dup MANE Select	NP_000340.2:n.651-247_651-245dup