Canonical Allele Identifier: CA39573453

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235677776dup , CM000663.2:g.235677776dup	GRCh38
NC_000001.10:g.235841076dup , CM000663.1:g.235841076dup	GRCh37
NC_000001.9:g.233907699dup	NCBI36
NG_007397.1:g.210870dup , LRG_143:g.210870dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.10801-152dup MANE Select	NP_000072.2:n.10801-152dup
ENST00000389793.7:c.10801-152dup MANE Select	ENSP00000374443.2:n.10801-152dup
NM_000081.3:c.10801-152dup , LRG_143t1:c.10801-152dup	NP_000072.2:n.10801-152dup
NM_001301365.1:c.10801-152dup , LRG_143t2:c.10801-152dup	NP_001288294.1:n.10801-152dup
ENST00000389793.6:c.10801-152dup	ENSP00000374443.2:n.10801-152dup
ENST00000389794.7:c.*6225-152dup	ENSP00000374444.4:n.*6225-152dup
ENST00000462376.2:n.2211-152dup
ENST00000473037.5:n.5791-152dup
ENST00000697178.1:c.*6496-152dup	ENSP00000513163.1:n.*6496-152dup
ENST00000697235.1:c.1351-152dup	ENSP00000513202.1:n.1351-152dup
ENST00000697236.1:c.4265-152dup	ENSP00000513203.1:n.4265-152dup
ENST00000697237.1:c.1512-152dup
ENST00000697239.1:n.195-152dup
ENST00000697240.1:c.2935-152dup	ENSP00000513205.1:n.2935-152dup
XM_011544031.1:c.10963-152dup	XP_011542333.1:n.10963-152dup
XM_011544032.1:c.10963-152dup	XP_011542334.1:n.10963-152dup
XM_011544033.1:c.10963-152dup	XP_011542335.1:n.10963-152dup
XM_011544033.2:c.10963-152dup	XP_011542335.1:n.10963-152dup
XM_011544034.1:c.10825-152dup	XP_011542336.1:n.10825-152dup
XM_011544036.1:c.8626-152dup	XP_011542338.1:n.8626-152dup
XM_011544036.2:c.8626-152dup	XP_011542338.1:n.8626-152dup
XM_017000150.1:c.10732-152dup	XP_016855639.1:n.10732-152dup