Canonical Allele Identifier: CA347113

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235712155_235712160del , CM000663.2:g.235712155_235712160del	GRCh38
NC_000001.10:g.235875455_235875460del , CM000663.1:g.235875455_235875460del	GRCh37
NC_000001.9:g.233942078_233942083del	NCBI36
NG_007397.1:g.176486_176491del , LRG_143:g.176486_176491del

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9827_9832del MANE Select	NP_000072.2:p.Asn3276_Thr3277del
ENST00000389793.7:c.9827_9832del MANE Select	ENSP00000374443.2:p.Asn3276_Thr3277del
NM_000081.3:c.9827_9832del , LRG_143t1:c.9827_9832del	NP_000072.2:p.Asn3276_Thr3277del
NM_001301365.1:c.9827_9832del , LRG_143t2:c.9827_9832del	NP_001288294.1:p.Asn3276_Thr3277del
ENST00000389793.6:c.9827_9832del	ENSP00000374443.2:p.Asn3276_Thr3277del
ENST00000389794.7:c.*5251_*5256del	ENSP00000374444.4:n.*5251_*5256del
ENST00000462376.1:n.246_251del
ENST00000462376.2:n.1237_1242del
ENST00000473037.5:n.4817_4822del
ENST00000697178.1:c.*5522_*5527del	ENSP00000513163.1:n.*5522_*5527del
ENST00000697179.1:n.2536_2541del
ENST00000697235.1:c.377_382del	ENSP00000513202.1:p.Asn126_Thr127del
ENST00000697236.1:c.3291_3296del	ENSP00000513203.1:n.3291_3296del
ENST00000697237.1:c.741-2951_741-2946del
ENST00000697240.1:c.1961_1966del	ENSP00000513205.1:p.Asn654_Thr655del
XM_011544031.1:c.9989_9994del	XP_011542333.1:p.Asn3330_Thr3331del
XM_011544032.1:c.9989_9994del	XP_011542334.1:p.Asn3330_Thr3331del
XM_011544033.1:c.9989_9994del	XP_011542335.1:p.Asn3330_Thr3331del
XM_011544033.2:c.9989_9994del	XP_011542335.1:p.Asn3330_Thr3331del
XM_011544034.1:c.9851_9856del	XP_011542336.1:p.Asn3284_Thr3285del
XM_011544036.1:c.7652_7657del	XP_011542338.1:p.Asn2551_Thr2552del
XM_011544036.2:c.7652_7657del	XP_011542338.1:p.Asn2551_Thr2552del
XM_017000150.1:c.9989_9994del	XP_016855639.1:p.Asn3330_Thr3331del