Canonical Allele Identifier: CA1465862

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235734607C>T , CM000663.2:g.235734607C>T	GRCh38
NC_000001.10:g.235897907C>T , CM000663.1:g.235897907C>T	GRCh37
NC_000001.9:g.233964530C>T	NCBI36
NG_007397.1:g.154034G>A , LRG_143:g.154034G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.8411G>A MANE Select	NP_000072.2:p.Gly2804Asp
ENST00000389793.7:c.8411G>A MANE Select	ENSP00000374443.2:p.Gly2804Asp
NM_000081.3:c.8411G>A , LRG_143t1:c.8411G>A	NP_000072.2:p.Gly2804Asp
NM_001301365.1:c.8411G>A , LRG_143t2:c.8411G>A	NP_001288294.1:p.Gly2804Asp
ENST00000389793.6:c.8411G>A	ENSP00000374443.2:p.Gly2804Asp
ENST00000389794.7:c.*3835G>A	ENSP00000374444.4:n.*3835G>A
ENST00000461526.2:c.3939G>A	ENSP00000513165.1:n.3939G>A
ENST00000473037.5:n.3401G>A
ENST00000475277.2:c.506G>A	ENSP00000513164.1:p.Gly169Asp
ENST00000697178.1:c.*3835G>A	ENSP00000513163.1:n.*3835G>A
ENST00000697236.1:c.2120G>A	ENSP00000513203.1:p.Gly707Asp
ENST00000697240.1:c.545G>A	ENSP00000513205.1:p.Gly182Asp
ENST00000697241.1:c.2891G>A	ENSP00000513206.1:p.Gly964Asp
XM_011544031.1:c.8573G>A	XP_011542333.1:p.Gly2858Asp
XM_011544032.1:c.8573G>A	XP_011542334.1:p.Gly2858Asp
XM_011544033.1:c.8573G>A	XP_011542335.1:p.Gly2858Asp
XM_011544033.2:c.8573G>A	XP_011542335.1:p.Gly2858Asp
XM_011544034.1:c.8435G>A	XP_011542336.1:p.Gly2812Asp
XM_011544035.1:c.8573G>A	XP_011542337.1:p.Gly2858Asp
XM_011544035.2:c.8573G>A	XP_011542337.1:p.Gly2858Asp
XM_011544036.1:c.6236G>A	XP_011542338.1:p.Gly2079Asp
XM_011544036.2:c.6236G>A	XP_011542338.1:p.Gly2079Asp
XM_017000150.1:c.8573G>A	XP_016855639.1:p.Gly2858Asp
XR_001736946.2:n.9608G>A
XR_001736947.1:n.9446G>A