Canonical Allele Identifier: CA352310711

Gene: STAC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36486191C>T , CM000665.2:g.36486191C>T	GRCh38
NC_000003.11:g.36527683C>T , CM000665.1:g.36527683C>T	GRCh37
NC_000003.10:g.36502687C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273183.8:c.629C>T MANE Select	ENSP00000273183.3:p.Ala210Val
ENST00000273183.7:c.629C>T	ENSP00000273183.3:p.Ala210Val
ENST00000427486.5:c.*196C>T	ENSP00000397521.1:n.*196C>T
ENST00000434649.1:c.413C>T	ENSP00000398403.1:p.Ala138Val
ENST00000457375.6:c.446C>T	ENSP00000393713.2:p.Ala149Val
ENST00000473452.1:n.21C>T
ENST00000476388.5:n.987C>T
NM_001292049.1:c.446C>T	NP_001278978.1:p.Ala149Val
NM_003149.2:c.629C>T	NP_003140.1:p.Ala210Val
XM_011534036.1:c.641C>T	XP_011532338.1:p.Ala214Val
XM_011534037.1:c.596C>T	XP_011532339.1:p.Ala199Val
XM_011534038.1:c.425C>T	XP_011532340.1:p.Ala142Val
XR_940496.1:n.990C>T
XM_011534037.3:c.596C>T	XP_011532339.1:p.Ala199Val
XM_011534038.2:c.425C>T	XP_011532340.1:p.Ala142Val
XM_017007083.1:c.425C>T	XP_016862572.1:p.Ala142Val
XM_024453722.1:c.641C>T	XP_024309490.1:p.Ala214Val
XM_024453723.1:c.458C>T	XP_024309491.1:p.Ala153Val
XR_940496.2:n.974C>T
NM_001292049.2:c.446C>T	NP_001278978.1:p.Ala149Val
NM_003149.3:c.629C>T MANE Select	NP_003140.1:p.Ala210Val