Canonical Allele Identifier: CA2686932493

Gene: STAR

Linked Data

• gnomAD v4: 8-38145553-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38145553T>C , CM000670.2:g.38145553T>C	GRCh38
NC_000008.10:g.38003071T>C , CM000670.1:g.38003071T>C	GRCh37
NC_000008.9:g.38122228T>C	NCBI36
NG_011827.1:g.10530A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276449.9:c.651-238A>G MANE Select	ENSP00000276449.3:n.651-238A>G
ENST00000276449.8:c.651-238A>G	ENSP00000276449.3:n.651-238A>G
ENST00000520114.1:n.1547A>G
ENST00000522050.1:c.586+410A>G
NM_000349.2:c.651-238A>G	NP_000340.2:n.651-238A>G
XM_006716392.1:c.650+410A>G	XP_006716455.1:n.650+410A>G
NM_000349.3:c.651-238A>G MANE Select	NP_000340.2:n.651-238A>G