Canonical Allele Identifier: CA2305064
Gene: STAC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36443616G>A , CM000665.2:g.36443616G>A GRCh38
NC_000003.11:g.36485108G>A , CM000665.1:g.36485108G>A GRCh37
NC_000003.10:g.36460112G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273183.8:c.364G>A MANE Select ENSP00000273183.3:p.Asp122Asn
ENST00000273183.7:c.364G>A ENSP00000273183.3:p.Asp122Asn
ENST00000427486.5:c.112-39376G>A ENSP00000397521.1:n.112-39376G>A
ENST00000434649.1:c.331G>A ENSP00000398403.1:p.Asp111Asn
ENST00000457375.6:c.364G>A ENSP00000393713.2:p.Asp122Asn
ENST00000476388.5:n.559G>A
ENST00000486143.1:n.323G>A
NM_001292049.1:c.364G>A NP_001278978.1:p.Asp122Asn
NM_003149.2:c.364G>A NP_003140.1:p.Asp122Asn
XM_011534036.1:c.376G>A XP_011532338.1:p.Asp126Asn
XM_011534037.1:c.331G>A XP_011532339.1:p.Asp111Asn
XM_011534038.1:c.160G>A XP_011532340.1:p.Asp54Asn
XR_940496.1:n.562G>A
XM_011534037.3:c.331G>A XP_011532339.1:p.Asp111Asn
XM_011534038.2:c.160G>A XP_011532340.1:p.Asp54Asn
XM_017007083.1:c.160G>A XP_016862572.1:p.Asp54Asn
XM_024453722.1:c.376G>A XP_024309490.1:p.Asp126Asn
XM_024453723.1:c.376G>A XP_024309491.1:p.Asp126Asn
XR_940496.2:n.546G>A
NM_001292049.2:c.364G>A NP_001278978.1:p.Asp122Asn
NM_003149.3:c.364G>A MANE Select NP_003140.1:p.Asp122Asn