Canonical Allele Identifier: CA2305035
Gene: STAC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.36443436C>A , CM000665.2:g.36443436C>A GRCh38
NC_000003.11:g.36484928C>A , CM000665.1:g.36484928C>A GRCh37
NC_000003.10:g.36459932C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000273183.8:c.184C>A MANE Select ENSP00000273183.3:p.Gln62Lys
ENST00000273183.7:c.184C>A ENSP00000273183.3:p.Gln62Lys
ENST00000427486.5:c.112-39556C>A ENSP00000397521.1:n.112-39556C>A
ENST00000434649.1:c.151C>A ENSP00000398403.1:p.Gln51Lys
ENST00000457375.6:c.184C>A ENSP00000393713.2:p.Gln62Lys
ENST00000476388.5:n.379C>A
ENST00000486143.1:n.143C>A
NM_001292049.1:c.184C>A NP_001278978.1:p.Gln62Lys
NM_003149.2:c.184C>A NP_003140.1:p.Gln62Lys
XM_011534036.1:c.196C>A XP_011532338.1:p.Gln66Lys
XM_011534037.1:c.151C>A XP_011532339.1:p.Gln51Lys
XM_011534038.1:c.-21C>A XP_011532340.1:n.-21C>A
XR_940496.1:n.382C>A
XM_011534037.3:c.151C>A XP_011532339.1:p.Gln51Lys
XM_011534038.2:c.-21C>A XP_011532340.1:n.-21C>A
XM_017007083.1:c.-21C>A XP_016862572.1:n.-21C>A
XM_024453722.1:c.196C>A XP_024309490.1:p.Gln66Lys
XM_024453723.1:c.196C>A XP_024309491.1:p.Gln66Lys
XR_940496.2:n.366C>A
NM_001292049.2:c.184C>A NP_001278978.1:p.Gln62Lys
NM_003149.3:c.184C>A MANE Select NP_003140.1:p.Gln62Lys