Canonical Allele Identifier: CA237754931

Gene: STAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57243911C>A , CM000674.2:g.57243911C>A	GRCh38
NC_000012.11:g.57637694C>A , CM000674.1:g.57637694C>A	GRCh37
NC_000012.10:g.55923961C>A	NCBI36
NG_033835.1:g.12283G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_145064.3:c.997-1G>T MANE Select	NP_659501.1:n.997-1G>T
ENST00000332782.7:c.997-1G>T MANE Select	ENSP00000329200.2:n.997-1G>T
NM_001286256.1:c.880-1G>T	NP_001273185.1:n.880-1G>T
NM_001286256.2:c.880-1G>T	NP_001273185.1:n.880-1G>T
NM_001286257.1:c.439-1G>T	NP_001273186.1:n.439-1G>T
NM_001286257.2:c.439-1G>T	NP_001273186.1:n.439-1G>T
NM_145064.2:c.997-1G>T	NP_659501.1:n.997-1G>T
NR_104422.1:n.699-1G>T
NR_104422.2:n.693-1G>T
ENST00000332782.6:c.997-1G>T	ENSP00000329200.2:n.997-1G>T
ENST00000546246.2:c.439-1G>T	ENSP00000441515.2:n.439-1G>T
ENST00000554578.5:c.880-1G>T	ENSP00000452068.1:n.880-1G>T
ENST00000557176.5:c.*57-1G>T	ENSP00000450740.1:n.*57-1G>T
XM_011538126.1:c.997-1G>T	XP_011536428.1:n.997-1G>T
XM_011538126.2:c.997-1G>T	XP_011536428.1:n.997-1G>T
XR_002957305.1:n.1296-1G>T
XR_944515.1:n.1126-1G>T
XR_944515.2:n.1126-1G>T