Canonical Allele Identifier: CA237756514

Gene: STAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57245143A>T , CM000674.2:g.57245143A>T	GRCh38
NC_000012.11:g.57638926A>T , CM000674.1:g.57638926A>T	GRCh37
NC_000012.10:g.55925193A>T	NCBI36
NG_033835.1:g.11051T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_145064.3:c.670+2T>A MANE Select	NP_659501.1:n.670+2T>A
ENST00000332782.7:c.670+2T>A MANE Select	ENSP00000329200.2:n.670+2T>A
NM_001286256.1:c.553+2T>A	NP_001273185.1:n.553+2T>A
NM_001286256.2:c.553+2T>A	NP_001273185.1:n.553+2T>A
NM_001286257.1:c.112+2T>A	NP_001273186.1:n.112+2T>A
NM_001286257.2:c.112+2T>A	NP_001273186.1:n.112+2T>A
NM_145064.2:c.670+2T>A	NP_659501.1:n.670+2T>A
NR_104422.1:n.373-178T>A
NR_104422.2:n.367-178T>A
ENST00000332782.6:c.670+2T>A	ENSP00000329200.2:n.670+2T>A
ENST00000546246.2:c.112+2T>A	ENSP00000441515.2:n.112+2T>A
ENST00000554003.1:n.404+2T>A
ENST00000554578.5:c.553+2T>A	ENSP00000452068.1:n.553+2T>A
ENST00000557176.5:c.46-178T>A	ENSP00000450740.1:n.46-178T>A
XM_011538126.1:c.670+2T>A	XP_011536428.1:n.670+2T>A
XM_011538126.2:c.670+2T>A	XP_011536428.1:n.670+2T>A
XR_002957305.1:n.800-178T>A
XR_944515.1:n.800-178T>A
XR_944515.2:n.800-178T>A