Canonical Allele Identifier: CA1465253

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235677195G>T , CM000663.2:g.235677195G>T	GRCh38
NC_000001.10:g.235840495G>T , CM000663.1:g.235840495G>T	GRCh37
NC_000001.9:g.233907118G>T	NCBI36
NG_007397.1:g.211446C>A , LRG_143:g.211446C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.2351-7C>A
ENST00000697178.1:c.*6920C>A	ENSP00000513163.1:n.*6920C>A
ENST00000697235.1:c.1491-7C>A	ENSP00000513202.1:n.1491-7C>A
ENST00000697236.1:c.4405-7C>A	ENSP00000513203.1:n.4405-7C>A
ENST00000697237.1:c.1652-7C>A
ENST00000697239.1:n.335-7C>A
ENST00000697240.1:c.3075-7C>A	ENSP00000513205.1:n.3075-7C>A
ENST00000389793.7:c.10941-7C>A MANE Select	ENSP00000374443.2:n.10941-7C>A
ENST00000389793.6:c.10941-7C>A	ENSP00000374443.2:n.10941-7C>A
ENST00000389794.7:c.*6365-7C>A	ENSP00000374444.4:n.*6365-7C>A
ENST00000473037.5:n.5931-7C>A
NM_000081.3:c.10941-7C>A , LRG_143t1:c.10941-7C>A	NP_000072.2:n.10941-7C>A
NM_001301365.1:c.10941-7C>A , LRG_143t2:c.10941-7C>A	NP_001288294.1:n.10941-7C>A
XM_011544031.1:c.11103-7C>A	XP_011542333.1:n.11103-7C>A
XM_011544032.1:c.11103-7C>A	XP_011542334.1:n.11103-7C>A
XM_011544033.1:c.11103-7C>A	XP_011542335.1:n.11103-7C>A
XM_011544034.1:c.10965-7C>A	XP_011542336.1:n.10965-7C>A
XM_011544036.1:c.8766-7C>A	XP_011542338.1:n.8766-7C>A
XM_011544033.2:c.11103-7C>A	XP_011542335.1:n.11103-7C>A
XM_011544036.2:c.8766-7C>A	XP_011542338.1:n.8766-7C>A
XM_017000150.1:c.10872-7C>A	XP_016855639.1:n.10872-7C>A
NM_000081.4:c.10941-7C>A MANE Select	NP_000072.2:n.10941-7C>A