Canonical Allele Identifier: CA344940775

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235716715G>T , CM000663.2:g.235716715G>T	GRCh38
NC_000001.10:g.235880015G>T , CM000663.1:g.235880015G>T	GRCh37
NC_000001.9:g.233946638G>T	NCBI36
NG_007397.1:g.171926C>A , LRG_143:g.171926C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9624C>A MANE Select	NP_000072.2:p.Tyr3208Ter
ENST00000389793.7:c.9624C>A MANE Select	ENSP00000374443.2:p.Tyr3208Ter
NM_000081.3:c.9624C>A , LRG_143t1:c.9624C>A	NP_000072.2:p.Tyr3208Ter
NM_001301365.1:c.9624C>A , LRG_143t2:c.9624C>A	NP_001288294.1:p.Tyr3208Ter
ENST00000389793.6:c.9624C>A	ENSP00000374443.2:p.Tyr3208Ter
ENST00000389794.7:c.*5048C>A	ENSP00000374444.4:n.*5048C>A
ENST00000461526.2:c.5152C>A	ENSP00000513165.1:n.5152C>A
ENST00000473037.5:n.4614C>A
ENST00000475277.1:n.490C>A
ENST00000475277.2:c.1719C>A	ENSP00000513164.1:p.Tyr573Ter
ENST00000697178.1:c.*5319C>A	ENSP00000513163.1:n.*5319C>A
ENST00000697235.1:c.174C>A	ENSP00000513202.1:p.Tyr58Ter
ENST00000697236.1:c.3088C>A	ENSP00000513203.1:n.3088C>A
ENST00000697237.1:c.580C>A
ENST00000697240.1:c.1758C>A	ENSP00000513205.1:p.Tyr586Ter
ENST00000697241.1:c.4104C>A	ENSP00000513206.1:p.Tyr1368Ter
XM_011544031.1:c.9786C>A	XP_011542333.1:p.Tyr3262Ter
XM_011544032.1:c.9786C>A	XP_011542334.1:p.Tyr3262Ter
XM_011544033.1:c.9786C>A	XP_011542335.1:p.Tyr3262Ter
XM_011544033.2:c.9786C>A	XP_011542335.1:p.Tyr3262Ter
XM_011544034.1:c.9648C>A	XP_011542336.1:p.Tyr3216Ter
XM_011544035.1:c.9786C>A	XP_011542337.1:p.Tyr3262Ter
XM_011544035.2:c.9786C>A	XP_011542337.1:p.Tyr3262Ter
XM_011544036.1:c.7449C>A	XP_011542338.1:p.Tyr2483Ter
XM_011544036.2:c.7449C>A	XP_011542338.1:p.Tyr2483Ter
XM_017000150.1:c.9786C>A	XP_016855639.1:p.Tyr3262Ter
XR_001736947.1:n.10659C>A