Canonical Allele Identifier: CA6647152

Gene: STAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57248705C>T , CM000674.2:g.57248705C>T	GRCh38
NC_000012.11:g.57642488C>T , CM000674.1:g.57642488C>T	GRCh37
NC_000012.10:g.55928755C>T	NCBI36
NG_033835.1:g.7489G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_145064.3:c.432+1G>A MANE Select	NP_659501.1:n.432+1G>A
ENST00000332782.7:c.432+1G>A MANE Select	ENSP00000329200.2:n.432+1G>A
NM_001286256.1:c.315+1G>A	NP_001273185.1:n.315+1G>A
NM_001286256.2:c.315+1G>A	NP_001273185.1:n.315+1G>A
NM_001286257.1:c.-126-507G>A	NP_001273186.1:n.-126-507G>A
NM_001286257.2:c.-126-507G>A	NP_001273186.1:n.-126-507G>A
NM_145064.2:c.432+1G>A	NP_659501.1:n.432+1G>A
NR_104422.1:n.202-507G>A
NR_104422.2:n.196-507G>A
ENST00000332782.6:c.432+1G>A	ENSP00000329200.2:n.432+1G>A
ENST00000546246.2:c.-126-507G>A	ENSP00000441515.2:n.-126-507G>A
ENST00000553489.1:c.432+1G>A	ENSP00000452299.1:n.432+1G>A
ENST00000554578.5:c.315+1G>A	ENSP00000452068.1:n.315+1G>A
ENST00000557176.5:c.-126-507G>A	ENSP00000450740.1:n.-126-507G>A
XM_011538126.1:c.432+1G>A	XP_011536428.1:n.432+1G>A
XM_011538126.2:c.432+1G>A	XP_011536428.1:n.432+1G>A
XR_002957305.1:n.628+1G>A
XR_944515.1:n.628+1G>A
XR_944515.2:n.628+1G>A