Canonical Allele Identifier: CA1465393

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235702776G>A , CM000663.2:g.235702776G>A	GRCh38
NC_000001.10:g.235866076G>A , CM000663.1:g.235866076G>A	GRCh37
NC_000001.9:g.233932699G>A	NCBI36
NG_007397.1:g.185865C>T , LRG_143:g.185865C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.1755C>T
ENST00000697178.1:c.*6040C>T	ENSP00000513163.1:n.*6040C>T
ENST00000697179.1:n.3054C>T
ENST00000697235.1:c.895C>T	ENSP00000513202.1:p.Arg299Ter
ENST00000697236.1:c.3809C>T	ENSP00000513203.1:n.3809C>T
ENST00000697237.1:c.1056C>T
ENST00000697240.1:c.2479C>T	ENSP00000513205.1:p.Arg827Ter
ENST00000389793.7:c.10345C>T MANE Select	ENSP00000374443.2:p.Arg3449Ter
ENST00000389793.6:c.10345C>T	ENSP00000374443.2:p.Arg3449Ter
ENST00000389794.7:c.*5769C>T	ENSP00000374444.4:n.*5769C>T
ENST00000473037.5:n.5335C>T
NM_000081.3:c.10345C>T , LRG_143t1:c.10345C>T	NP_000072.2:p.Arg3449Ter
NM_001301365.1:c.10345C>T , LRG_143t2:c.10345C>T	NP_001288294.1:p.Arg3449Ter
XM_011544031.1:c.10507C>T	XP_011542333.1:p.Arg3503Ter
XM_011544032.1:c.10507C>T	XP_011542334.1:p.Arg3503Ter
XM_011544033.1:c.10507C>T	XP_011542335.1:p.Arg3503Ter
XM_011544034.1:c.10369C>T	XP_011542336.1:p.Arg3457Ter
XM_011544036.1:c.8170C>T	XP_011542338.1:p.Arg2724Ter
XM_011544033.2:c.10507C>T	XP_011542335.1:p.Arg3503Ter
XM_011544036.2:c.8170C>T	XP_011542338.1:p.Arg2724Ter
XM_017000150.1:c.10306-5504C>T	XP_016855639.1:n.10306-5504C>T
NM_000081.4:c.10345C>T MANE Select	NP_000072.2:p.Arg3449Ter