Canonical Allele Identifier: CA1465295

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235687009C>T , CM000663.2:g.235687009C>T	GRCh38
NC_000001.10:g.235850309C>T , CM000663.1:g.235850309C>T	GRCh37
NC_000001.9:g.233916932C>T	NCBI36
NG_007397.1:g.201632G>A , LRG_143:g.201632G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.10740G>A MANE Select	NP_000072.2:p.Leu3580=
ENST00000389793.7:c.10740G>A MANE Select	ENSP00000374443.2:p.Leu3580=
NM_000081.3:c.10740G>A , LRG_143t1:c.10740G>A	NP_000072.2:p.Leu3580=
NM_001301365.1:c.10740G>A , LRG_143t2:c.10740G>A	NP_001288294.1:p.Leu3580=
ENST00000389793.6:c.10740G>A	ENSP00000374443.2:p.Leu3580=
ENST00000389794.7:c.*6164G>A	ENSP00000374444.4:n.*6164G>A
ENST00000462376.2:n.2150G>A
ENST00000473037.5:n.5730G>A
ENST00000697178.1:c.*6435G>A	ENSP00000513163.1:n.*6435G>A
ENST00000697235.1:c.1290G>A	ENSP00000513202.1:p.Leu430=
ENST00000697236.1:c.4204G>A	ENSP00000513203.1:n.4204G>A
ENST00000697237.1:c.1451G>A
ENST00000697239.1:n.134G>A
ENST00000697240.1:c.2874G>A	ENSP00000513205.1:p.Leu958=
XM_011544031.1:c.10902G>A	XP_011542333.1:p.Leu3634=
XM_011544032.1:c.10902G>A	XP_011542334.1:p.Leu3634=
XM_011544033.1:c.10902G>A	XP_011542335.1:p.Leu3634=
XM_011544033.2:c.10902G>A	XP_011542335.1:p.Leu3634=
XM_011544034.1:c.10764G>A	XP_011542336.1:p.Leu3588=
XM_011544036.1:c.8565G>A	XP_011542338.1:p.Leu2855=
XM_011544036.2:c.8565G>A	XP_011542338.1:p.Leu2855=
XM_017000150.1:c.10671G>A	XP_016855639.1:p.Leu3557=