Canonical Allele Identifier: CA1465440

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235709078_235709079del , CM000663.2:g.235709078_235709079del	GRCh38
NC_000001.10:g.235872378_235872379del , CM000663.1:g.235872378_235872379del	GRCh37
NC_000001.9:g.233939001_233939002del	NCBI36
NG_007397.1:g.179564_179565del , LRG_143:g.179564_179565del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.1553+14_1553+15del
ENST00000697178.1:c.*5838+14_*5838+15del	ENSP00000513163.1:n.*5838+14_*5838+15del
ENST00000697179.1:n.2852+14_2852+15del
ENST00000697235.1:c.693+14_693+15del	ENSP00000513202.1:n.693+14_693+15del
ENST00000697236.1:c.3607+14_3607+15del	ENSP00000513203.1:n.3607+14_3607+15del
ENST00000697237.1:c.854+14_854+15del
ENST00000697240.1:c.2277+14_2277+15del	ENSP00000513205.1:n.2277+14_2277+15del
ENST00000389793.7:c.10143+14_10143+15del MANE Select	ENSP00000374443.2:n.10143+14_10143+15del
ENST00000389793.6:c.10143+14_10143+15del	ENSP00000374443.2:n.10143+14_10143+15del
ENST00000389794.7:c.*5567+14_*5567+15del	ENSP00000374444.4:n.*5567+14_*5567+15del
ENST00000473037.5:n.5133+14_5133+15del
NM_000081.3:c.10143+14_10143+15del , LRG_143t1:c.10143+14_10143+15del	NP_000072.2:n.10143+14_10143+15del
NM_001301365.1:c.10143+14_10143+15del , LRG_143t2:c.10143+14_10143+15del	NP_001288294.1:n.10143+14_10143+15del
XM_011544031.1:c.10305+14_10305+15del	XP_011542333.1:n.10305+14_10305+15del
XM_011544032.1:c.10305+14_10305+15del	XP_011542334.1:n.10305+14_10305+15del
XM_011544033.1:c.10305+14_10305+15del	XP_011542335.1:n.10305+14_10305+15del
XM_011544034.1:c.10167+14_10167+15del	XP_011542336.1:n.10167+14_10167+15del
XM_011544036.1:c.7968+14_7968+15del	XP_011542338.1:n.7968+14_7968+15del
XM_011544033.2:c.10305+14_10305+15del	XP_011542335.1:n.10305+14_10305+15del
XM_011544036.2:c.7968+14_7968+15del	XP_011542338.1:n.7968+14_7968+15del
XM_017000150.1:c.10305+14_10305+15del	XP_016855639.1:n.10305+14_10305+15del
NM_000081.4:c.10143+14_10143+15del MANE Select	NP_000072.2:n.10143+14_10143+15del