Canonical Allele Identifier: CA2305091

Gene: STAC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36483015C>T , CM000665.2:g.36483015C>T	GRCh38
NC_000003.11:g.36524507C>T , CM000665.1:g.36524507C>T	GRCh37
NC_000003.10:g.36499511C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273183.8:c.412C>T MANE Select	ENSP00000273183.3:p.Arg138Cys
ENST00000273183.7:c.412C>T	ENSP00000273183.3:p.Arg138Cys
ENST00000427486.5:c.135C>T	ENSP00000397521.1:p.Cys45=
ENST00000434649.1:c.356-3119C>T	ENSP00000398403.1:n.356-3119C>T
ENST00000457375.6:c.389-3119C>T	ENSP00000393713.2:n.389-3119C>T
ENST00000476388.5:n.607C>T
NM_001292049.1:c.389-3119C>T	NP_001278978.1:n.389-3119C>T
NM_003149.2:c.412C>T	NP_003140.1:p.Arg138Cys
XM_011534036.1:c.424C>T	XP_011532338.1:p.Arg142Cys
XM_011534037.1:c.379C>T	XP_011532339.1:p.Arg127Cys
XM_011534038.1:c.208C>T	XP_011532340.1:p.Arg70Cys
XR_940496.1:n.610C>T
XM_011534037.3:c.379C>T	XP_011532339.1:p.Arg127Cys
XM_011534038.2:c.208C>T	XP_011532340.1:p.Arg70Cys
XM_017007083.1:c.208C>T	XP_016862572.1:p.Arg70Cys
XM_024453722.1:c.424C>T	XP_024309490.1:p.Arg142Cys
XM_024453723.1:c.401-3119C>T	XP_024309491.1:n.401-3119C>T
XR_940496.2:n.594C>T
NM_001292049.2:c.389-3119C>T	NP_001278978.1:n.389-3119C>T
NM_003149.3:c.412C>T MANE Select	NP_003140.1:p.Arg138Cys