Canonical Allele Identifier: CA344944453

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235720888G>C , CM000663.2:g.235720888G>C	GRCh38
NC_000001.10:g.235884188G>C , CM000663.1:g.235884188G>C	GRCh37
NC_000001.9:g.233950811G>C	NCBI36
NG_007397.1:g.167753C>G , LRG_143:g.167753C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9333C>G MANE Select	NP_000072.2:p.Tyr3111Ter
ENST00000389793.7:c.9333C>G MANE Select	ENSP00000374443.2:p.Tyr3111Ter
NM_000081.3:c.9333C>G , LRG_143t1:c.9333C>G	NP_000072.2:p.Tyr3111Ter
NM_001301365.1:c.9333C>G , LRG_143t2:c.9333C>G	NP_001288294.1:p.Tyr3111Ter
ENST00000389793.6:c.9333C>G	ENSP00000374443.2:p.Tyr3111Ter
ENST00000389794.7:c.*4757C>G	ENSP00000374444.4:n.*4757C>G
ENST00000461526.2:c.4861C>G	ENSP00000513165.1:n.4861C>G
ENST00000473037.5:n.4323C>G
ENST00000475277.1:n.199C>G
ENST00000475277.2:c.1428C>G	ENSP00000513164.1:p.Tyr476Ter
ENST00000697178.1:c.*4757C>G	ENSP00000513163.1:n.*4757C>G
ENST00000697235.1:c.3C>G	ENSP00000513202.1:p.Tyr1Ter
ENST00000697236.1:c.3024+3140C>G	ENSP00000513203.1:n.3024+3140C>G
ENST00000697237.1:c.289C>G
ENST00000697240.1:c.1467C>G	ENSP00000513205.1:p.Tyr489Ter
ENST00000697241.1:c.3813C>G	ENSP00000513206.1:p.Tyr1271Ter
XM_011544031.1:c.9495C>G	XP_011542333.1:p.Tyr3165Ter
XM_011544032.1:c.9495C>G	XP_011542334.1:p.Tyr3165Ter
XM_011544033.1:c.9495C>G	XP_011542335.1:p.Tyr3165Ter
XM_011544033.2:c.9495C>G	XP_011542335.1:p.Tyr3165Ter
XM_011544034.1:c.9357C>G	XP_011542336.1:p.Tyr3119Ter
XM_011544035.1:c.9495C>G	XP_011542337.1:p.Tyr3165Ter
XM_011544035.2:c.9495C>G	XP_011542337.1:p.Tyr3165Ter
XM_011544036.1:c.7158C>G	XP_011542338.1:p.Tyr2386Ter
XM_011544036.2:c.7158C>G	XP_011542338.1:p.Tyr2386Ter
XM_017000150.1:c.9495C>G	XP_016855639.1:p.Tyr3165Ter
XR_001736947.1:n.10368C>G