Canonical Allele Identifier: CA1465933

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235741636C>T , CM000663.2:g.235741636C>T	GRCh38
NC_000001.10:g.235904936C>T , CM000663.1:g.235904936C>T	GRCh37
NC_000001.9:g.233971559C>T	NCBI36
NG_007397.1:g.147005G>A , LRG_143:g.147005G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.8152-8G>A MANE Select	NP_000072.2:n.8152-8G>A
ENST00000389793.7:c.8152-8G>A MANE Select	ENSP00000374443.2:n.8152-8G>A
NM_000081.3:c.8152-8G>A , LRG_143t1:c.8152-8G>A	NP_000072.2:n.8152-8G>A
NM_001301365.1:c.8152-8G>A , LRG_143t2:c.8152-8G>A	NP_001288294.1:n.8152-8G>A
ENST00000389793.6:c.8152-8G>A	ENSP00000374443.2:n.8152-8G>A
ENST00000389794.7:c.*3576-8G>A	ENSP00000374444.4:n.*3576-8G>A
ENST00000461526.1:n.55-8G>A
ENST00000461526.2:c.2827-8G>A	ENSP00000513165.1:n.2827-8G>A
ENST00000475277.2:c.247-8G>A	ENSP00000513164.1:n.247-8G>A
ENST00000697178.1:c.*3576-8G>A	ENSP00000513163.1:n.*3576-8G>A
ENST00000697236.1:c.1861-8G>A	ENSP00000513203.1:n.1861-8G>A
ENST00000697240.1:c.286-8G>A	ENSP00000513205.1:n.286-8G>A
ENST00000697241.1:c.2632-8G>A	ENSP00000513206.1:n.2632-8G>A
XM_011544031.1:c.8314-8G>A	XP_011542333.1:n.8314-8G>A
XM_011544032.1:c.8314-8G>A	XP_011542334.1:n.8314-8G>A
XM_011544033.1:c.8314-8G>A	XP_011542335.1:n.8314-8G>A
XM_011544033.2:c.8314-8G>A	XP_011542335.1:n.8314-8G>A
XM_011544034.1:c.8176-8G>A	XP_011542336.1:n.8176-8G>A
XM_011544035.1:c.8314-8G>A	XP_011542337.1:n.8314-8G>A
XM_011544035.2:c.8314-8G>A	XP_011542337.1:n.8314-8G>A
XM_011544036.1:c.5977-8G>A	XP_011542338.1:n.5977-8G>A
XM_011544036.2:c.5977-8G>A	XP_011542338.1:n.5977-8G>A
XM_011544037.1:c.8314-8G>A	XP_011542339.1:n.8314-8G>A
XM_011544037.2:c.8314-8G>A	XP_011542339.1:n.8314-8G>A
XM_011544038.1:c.8314-8G>A	XP_011542340.1:n.8314-8G>A
XM_017000150.1:c.8314-8G>A	XP_016855639.1:n.8314-8G>A
XR_001736946.2:n.8496-8G>A
XR_001736947.1:n.8334-8G>A
XR_001736948.1:n.7783-8G>A