Canonical Allele Identifier: CA2305040

Gene: STAC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36443481G>A , CM000665.2:g.36443481G>A	GRCh38
NC_000003.11:g.36484973G>A , CM000665.1:g.36484973G>A	GRCh37
NC_000003.10:g.36459977G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273183.8:c.229G>A MANE Select	ENSP00000273183.3:p.Ala77Thr
ENST00000273183.7:c.229G>A	ENSP00000273183.3:p.Ala77Thr
ENST00000427486.5:c.112-39511G>A	ENSP00000397521.1:n.112-39511G>A
ENST00000434649.1:c.196G>A	ENSP00000398403.1:p.Ala66Thr
ENST00000457375.6:c.229G>A	ENSP00000393713.2:p.Ala77Thr
ENST00000476388.5:n.424G>A
ENST00000486143.1:n.188G>A
NM_001292049.1:c.229G>A	NP_001278978.1:p.Ala77Thr
NM_003149.2:c.229G>A	NP_003140.1:p.Ala77Thr
XM_011534036.1:c.241G>A	XP_011532338.1:p.Ala81Thr
XM_011534037.1:c.196G>A	XP_011532339.1:p.Ala66Thr
XM_011534038.1:c.25G>A	XP_011532340.1:p.Ala9Thr
XR_940496.1:n.427G>A
XM_011534037.3:c.196G>A	XP_011532339.1:p.Ala66Thr
XM_011534038.2:c.25G>A	XP_011532340.1:p.Ala9Thr
XM_017007083.1:c.25G>A	XP_016862572.1:p.Ala9Thr
XM_024453722.1:c.241G>A	XP_024309490.1:p.Ala81Thr
XM_024453723.1:c.241G>A	XP_024309491.1:p.Ala81Thr
XR_940496.2:n.411G>A
NM_001292049.2:c.229G>A	NP_001278978.1:p.Ala77Thr
NM_003149.3:c.229G>A MANE Select	NP_003140.1:p.Ala77Thr