Canonical Allele Identifier: CA2305279

Gene: STAC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.36505774T>C , CM000665.2:g.36505774T>C	GRCh38
NC_000003.11:g.36547266T>C , CM000665.1:g.36547266T>C	GRCh37
NC_000003.10:g.36522270T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273183.8:c.860T>C MANE Select	ENSP00000273183.3:p.Met287Thr
ENST00000273183.7:c.860T>C	ENSP00000273183.3:p.Met287Thr
ENST00000434649.1:c.644T>C	ENSP00000398403.1:p.Met215Thr
ENST00000457375.6:c.677T>C	ENSP00000393713.2:p.Met226Thr
ENST00000473452.1:n.252T>C
ENST00000476388.5:n.1218T>C
NM_001292049.1:c.677T>C	NP_001278978.1:p.Met226Thr
NM_003149.2:c.860T>C	NP_003140.1:p.Met287Thr
XM_011534036.1:c.872T>C	XP_011532338.1:p.Met291Thr
XM_011534037.1:c.827T>C	XP_011532339.1:p.Met276Thr
XM_011534038.1:c.656T>C	XP_011532340.1:p.Met219Thr
XM_011534037.3:c.827T>C	XP_011532339.1:p.Met276Thr
XM_011534038.2:c.656T>C	XP_011532340.1:p.Met219Thr
XM_017007083.1:c.656T>C	XP_016862572.1:p.Met219Thr
XM_024453722.1:c.872T>C	XP_024309490.1:p.Met291Thr
XM_024453723.1:c.689T>C	XP_024309491.1:p.Met230Thr
NM_001292049.2:c.677T>C	NP_001278978.1:p.Met226Thr
NM_003149.3:c.860T>C MANE Select	NP_003140.1:p.Met287Thr