Canonical Allele Identifier: CA344922059

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235677598T>A , CM000663.2:g.235677598T>A	GRCh38
NC_000001.10:g.235840898T>A , CM000663.1:g.235840898T>A	GRCh37
NC_000001.9:g.233907521T>A	NCBI36
NG_007397.1:g.211043A>T , LRG_143:g.211043A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.10822A>T MANE Select	NP_000072.2:p.Thr3608Ser
ENST00000389793.7:c.10822A>T MANE Select	ENSP00000374443.2:p.Thr3608Ser
NM_000081.3:c.10822A>T , LRG_143t1:c.10822A>T	NP_000072.2:p.Thr3608Ser
NM_001301365.1:c.10822A>T , LRG_143t2:c.10822A>T	NP_001288294.1:p.Thr3608Ser
ENST00000389793.6:c.10822A>T	ENSP00000374443.2:p.Thr3608Ser
ENST00000389794.7:c.*6246A>T	ENSP00000374444.4:n.*6246A>T
ENST00000462376.2:n.2232A>T
ENST00000473037.5:n.5812A>T
ENST00000697178.1:c.*6517A>T	ENSP00000513163.1:n.*6517A>T
ENST00000697235.1:c.1372A>T	ENSP00000513202.1:p.Thr458Ser
ENST00000697236.1:c.4286A>T	ENSP00000513203.1:n.4286A>T
ENST00000697237.1:c.1533A>T
ENST00000697239.1:n.216A>T
ENST00000697240.1:c.2956A>T	ENSP00000513205.1:p.Thr986Ser
XM_011544031.1:c.10984A>T	XP_011542333.1:p.Thr3662Ser
XM_011544032.1:c.10984A>T	XP_011542334.1:p.Thr3662Ser
XM_011544033.1:c.10984A>T	XP_011542335.1:p.Thr3662Ser
XM_011544033.2:c.10984A>T	XP_011542335.1:p.Thr3662Ser
XM_011544034.1:c.10846A>T	XP_011542336.1:p.Thr3616Ser
XM_011544036.1:c.8647A>T	XP_011542338.1:p.Thr2883Ser
XM_011544036.2:c.8647A>T	XP_011542338.1:p.Thr2883Ser
XM_017000150.1:c.10753A>T	XP_016855639.1:p.Thr3585Ser