Canonical Allele Identifier: CA1465997

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235746397C>T , CM000663.2:g.235746397C>T	GRCh38
NC_000001.10:g.235909697C>T , CM000663.1:g.235909697C>T	GRCh37
NC_000001.9:g.233976320C>T	NCBI36
NG_007397.1:g.142244G>A , LRG_143:g.142244G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.7911G>A MANE Select	NP_000072.2:p.Thr2637=
ENST00000389793.7:c.7911G>A MANE Select	ENSP00000374443.2:p.Thr2637=
NM_000081.3:c.7911G>A , LRG_143t1:c.7911G>A	NP_000072.2:p.Thr2637=
NM_001301365.1:c.7911G>A , LRG_143t2:c.7911G>A	NP_001288294.1:p.Thr2637=
ENST00000389793.6:c.7911G>A	ENSP00000374443.2:p.Thr2637=
ENST00000389794.7:c.*3335G>A	ENSP00000374444.4:n.*3335G>A
ENST00000461526.2:c.2586G>A	ENSP00000513165.1:p.Thr862=
ENST00000475277.2:c.6G>A	ENSP00000513164.1:p.Thr2=
ENST00000697178.1:c.*3335G>A	ENSP00000513163.1:n.*3335G>A
ENST00000697236.1:c.1620G>A	ENSP00000513203.1:p.Thr540=
ENST00000697240.1:c.45G>A	ENSP00000513205.1:p.Thr15=
ENST00000697241.1:c.2391G>A	ENSP00000513206.1:p.Thr797=
XM_011544031.1:c.8073G>A	XP_011542333.1:p.Thr2691=
XM_011544032.1:c.8073G>A	XP_011542334.1:p.Thr2691=
XM_011544033.1:c.8073G>A	XP_011542335.1:p.Thr2691=
XM_011544033.2:c.8073G>A	XP_011542335.1:p.Thr2691=
XM_011544034.1:c.7935G>A	XP_011542336.1:p.Thr2645=
XM_011544035.1:c.8073G>A	XP_011542337.1:p.Thr2691=
XM_011544035.2:c.8073G>A	XP_011542337.1:p.Thr2691=
XM_011544036.1:c.5736G>A	XP_011542338.1:p.Thr1912=
XM_011544036.2:c.5736G>A	XP_011542338.1:p.Thr1912=
XM_011544037.1:c.8073G>A	XP_011542339.1:p.Thr2691=
XM_011544037.2:c.8073G>A	XP_011542339.1:p.Thr2691=
XM_011544038.1:c.8073G>A	XP_011542340.1:p.Thr2691=
XM_017000150.1:c.8073G>A	XP_016855639.1:p.Thr2691=
XR_001736946.2:n.8255G>A
XR_001736947.1:n.8093G>A
XR_001736948.1:n.7542G>A