Canonical Allele Identifier: CA581430333

Gene: STAR

Linked Data

• dbSNP Id: rs1457447771
• gnomAD v2: 8-38003783-C-CG
• gnomAD v4: 8-38146265-C-CG
• MyVariant Identifiers: chr8:g.38003783_38003784insG (hg19) ; chr8:g.38146265_38146266insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38146265_38146266insG , CM000670.2:g.38146265_38146266insG	GRCh38
NC_000008.10:g.38003783_38003784insG , CM000670.1:g.38003783_38003784insG	GRCh37
NC_000008.9:g.38122940_38122941insG	NCBI36
NG_011827.1:g.9817_9818insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.465+23_465+24insC MANE Select	ENSP00000276449.3:n.465+23_465+24insC
ENST00000276449.8:c.465+23_465+24insC	ENSP00000276449.3:n.465+23_465+24insC
ENST00000520114.1:n.952+23_952+24insC
ENST00000522050.1:c.401+23_401+24insC
NM_000349.2:c.465+23_465+24insC	NP_000340.2:n.465+23_465+24insC
XM_006716392.1:c.465+23_465+24insC	XP_006716455.1:n.465+23_465+24insC
NM_000349.3:c.465+23_465+24insC MANE Select	NP_000340.2:n.465+23_465+24insC