Canonical Allele Identifier: CA39604448

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235741469G>T , CM000663.2:g.235741469G>T	GRCh38
NC_000001.10:g.235904769G>T , CM000663.1:g.235904769G>T	GRCh37
NC_000001.9:g.233971392G>T	NCBI36
NG_007397.1:g.147172C>A , LRG_143:g.147172C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.2986C>A	ENSP00000513165.1:p.Pro996Thr
ENST00000475277.2:c.406C>A	ENSP00000513164.1:p.Pro136Thr
ENST00000697178.1:c.*3735C>A	ENSP00000513163.1:n.*3735C>A
ENST00000697236.1:c.2020C>A	ENSP00000513203.1:p.Pro674Thr
ENST00000697240.1:c.445C>A	ENSP00000513205.1:p.Pro149Thr
ENST00000697241.1:c.2791C>A	ENSP00000513206.1:p.Pro931Thr
ENST00000389793.7:c.8311C>A MANE Select	ENSP00000374443.2:p.Pro2771Thr
ENST00000389793.6:c.8311C>A	ENSP00000374443.2:p.Pro2771Thr
ENST00000389794.7:c.*3735C>A	ENSP00000374444.4:n.*3735C>A
ENST00000461526.1:n.214C>A
NM_000081.3:c.8311C>A , LRG_143t1:c.8311C>A	NP_000072.2:p.Pro2771Thr
NM_001301365.1:c.8311C>A , LRG_143t2:c.8311C>A	NP_001288294.1:p.Pro2771Thr
XM_011544031.1:c.8473C>A	XP_011542333.1:p.Pro2825Thr
XM_011544032.1:c.8473C>A	XP_011542334.1:p.Pro2825Thr
XM_011544033.1:c.8473C>A	XP_011542335.1:p.Pro2825Thr
XM_011544034.1:c.8335C>A	XP_011542336.1:p.Pro2779Thr
XM_011544035.1:c.8473C>A	XP_011542337.1:p.Pro2825Thr
XM_011544036.1:c.6136C>A	XP_011542338.1:p.Pro2046Thr
XM_011544037.1:c.8473C>A	XP_011542339.1:p.Pro2825Thr
XM_011544038.1:c.8473C>A	XP_011542340.1:p.Pro2825Thr
XM_011544033.2:c.8473C>A	XP_011542335.1:p.Pro2825Thr
XM_011544035.2:c.8473C>A	XP_011542337.1:p.Pro2825Thr
XM_011544036.2:c.6136C>A	XP_011542338.1:p.Pro2046Thr
XM_011544037.2:c.8473C>A	XP_011542339.1:p.Pro2825Thr
XM_017000150.1:c.8473C>A	XP_016855639.1:p.Pro2825Thr
XR_001736946.2:n.8655C>A
XR_001736947.1:n.8493C>A
XR_001736948.1:n.7942C>A
NM_000081.4:c.8311C>A MANE Select	NP_000072.2:p.Pro2771Thr