Canonical Allele Identifier: CA344924856

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235744050G>A , CM000663.2:g.235744050G>A	GRCh38
NC_000001.10:g.235907350G>A , CM000663.1:g.235907350G>A	GRCh37
NC_000001.9:g.233973973G>A	NCBI36
NG_007397.1:g.144591C>T , LRG_143:g.144591C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.2755C>T	ENSP00000513165.1:p.Gln919Ter
ENST00000475277.2:c.175C>T	ENSP00000513164.1:p.Gln59Ter
ENST00000697178.1:c.*3504C>T	ENSP00000513163.1:n.*3504C>T
ENST00000697236.1:c.1789C>T	ENSP00000513203.1:p.Gln597Ter
ENST00000697240.1:c.214C>T	ENSP00000513205.1:p.Gln72Ter
ENST00000697241.1:c.2560C>T	ENSP00000513206.1:p.Gln854Ter
ENST00000389793.7:c.8080C>T MANE Select	ENSP00000374443.2:p.Gln2694Ter
ENST00000389793.6:c.8080C>T	ENSP00000374443.2:p.Gln2694Ter
ENST00000389794.7:c.*3504C>T	ENSP00000374444.4:n.*3504C>T
NM_000081.3:c.8080C>T , LRG_143t1:c.8080C>T	NP_000072.2:p.Gln2694Ter
NM_001301365.1:c.8080C>T , LRG_143t2:c.8080C>T	NP_001288294.1:p.Gln2694Ter
XM_011544031.1:c.8242C>T	XP_011542333.1:p.Gln2748Ter
XM_011544032.1:c.8242C>T	XP_011542334.1:p.Gln2748Ter
XM_011544033.1:c.8242C>T	XP_011542335.1:p.Gln2748Ter
XM_011544034.1:c.8104C>T	XP_011542336.1:p.Gln2702Ter
XM_011544035.1:c.8242C>T	XP_011542337.1:p.Gln2748Ter
XM_011544036.1:c.5905C>T	XP_011542338.1:p.Gln1969Ter
XM_011544037.1:c.8242C>T	XP_011542339.1:p.Gln2748Ter
XM_011544038.1:c.8242C>T	XP_011542340.1:p.Gln2748Ter
XM_011544033.2:c.8242C>T	XP_011542335.1:p.Gln2748Ter
XM_011544035.2:c.8242C>T	XP_011542337.1:p.Gln2748Ter
XM_011544036.2:c.5905C>T	XP_011542338.1:p.Gln1969Ter
XM_011544037.2:c.8242C>T	XP_011542339.1:p.Gln2748Ter
XM_017000150.1:c.8242C>T	XP_016855639.1:p.Gln2748Ter
XR_001736946.2:n.8424C>T
XR_001736947.1:n.8262C>T
XR_001736948.1:n.7711C>T
NM_000081.4:c.8080C>T MANE Select	NP_000072.2:p.Gln2694Ter