Canonical Allele Identifier: CA923726343

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235759295_235759300del , CM000663.2:g.235759295_235759300del	GRCh38
NC_000001.10:g.235922595_235922600del , CM000663.1:g.235922595_235922600del	GRCh37
NC_000001.9:g.233989218_233989223del	NCBI36
NG_007397.1:g.129344_129349del , LRG_143:g.129344_129349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.1231_1236del	ENSP00000513165.1:p.Ser411_Val412del
ENST00000697178.1:c.*1980_*1985del	ENSP00000513163.1:n.*1980_*1985del
ENST00000697236.1:c.265_270del	ENSP00000513203.1:p.Ser89_Val90del
ENST00000697241.1:c.988_993del	ENSP00000513206.1:p.Ser330_Val331del
ENST00000389793.7:c.6556_6561del MANE Select	ENSP00000374443.2:p.Ser2186_Val2187del
ENST00000389793.6:c.6556_6561del	ENSP00000374443.2:p.Ser2186_Val2187del
ENST00000389794.7:c.*1980_*1985del	ENSP00000374444.4:n.*1980_*1985del
ENST00000489585.5:n.6947_6952del
NM_000081.3:c.6556_6561del , LRG_143t1:c.6556_6561del	NP_000072.2:p.Ser2186_Val2187del
NM_001301365.1:c.6556_6561del , LRG_143t2:c.6556_6561del	NP_001288294.1:p.Ser2186_Val2187del
XM_011544031.1:c.6556_6561del	XP_011542333.1:p.Ser2186_Val2187del
XM_011544032.1:c.6556_6561del	XP_011542334.1:p.Ser2186_Val2187del
XM_011544033.1:c.6556_6561del	XP_011542335.1:p.Ser2186_Val2187del
XM_011544034.1:c.6418_6423del	XP_011542336.1:p.Ser2140_Val2141del
XM_011544035.1:c.6556_6561del	XP_011542337.1:p.Ser2186_Val2187del
XM_011544036.1:c.4219_4224del	XP_011542338.1:p.Ser1407_Val1408del
XM_011544037.1:c.6556_6561del	XP_011542339.1:p.Ser2186_Val2187del
XM_011544038.1:c.6556_6561del	XP_011542340.1:p.Ser2186_Val2187del
XM_011544039.1:c.6556_6561del	XP_011542341.1:p.Ser2186_Val2187del
XM_011544033.2:c.6556_6561del	XP_011542335.1:p.Ser2186_Val2187del
XM_011544035.2:c.6556_6561del	XP_011542337.1:p.Ser2186_Val2187del
XM_011544036.2:c.4219_4224del	XP_011542338.1:p.Ser1407_Val1408del
XM_011544037.2:c.6556_6561del	XP_011542339.1:p.Ser2186_Val2187del
XM_011544039.2:c.6556_6561del	XP_011542341.1:p.Ser2186_Val2187del
XM_017000150.1:c.6556_6561del	XP_016855639.1:p.Ser2186_Val2187del
XR_001736946.2:n.6738_6743del
XR_001736947.1:n.6738_6743del
XR_001736948.1:n.6738_6743del
NM_000081.4:c.6556_6561del MANE Select	NP_000072.2:p.Ser2186_Val2187del