Canonical Allele Identifier: CA1466695

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235781018A>G , CM000663.2:g.235781018A>G	GRCh38
NC_000001.10:g.235944318A>G , CM000663.1:g.235944318A>G	GRCh37
NC_000001.9:g.234010941A>G	NCBI36
NG_007397.1:g.107623T>C , LRG_143:g.107623T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697178.1:c.*485T>C	ENSP00000513163.1:n.*485T>C
ENST00000389793.7:c.5061T>C MANE Select	ENSP00000374443.2:p.Tyr1687=
ENST00000389793.6:c.5061T>C	ENSP00000374443.2:p.Tyr1687=
ENST00000389794.7:c.*485T>C	ENSP00000374444.4:n.*485T>C
ENST00000489585.5:n.5612T>C
NM_000081.3:c.5061T>C , LRG_143t1:c.5061T>C	NP_000072.2:p.Tyr1687=
NM_001301365.1:c.5061T>C , LRG_143t2:c.5061T>C	NP_001288294.1:p.Tyr1687=
XM_011544031.1:c.5061T>C	XP_011542333.1:p.Tyr1687=
XM_011544032.1:c.5061T>C	XP_011542334.1:p.Tyr1687=
XM_011544033.1:c.5061T>C	XP_011542335.1:p.Tyr1687=
XM_011544034.1:c.5061T>C	XP_011542336.1:p.Tyr1687=
XM_011544035.1:c.5061T>C	XP_011542337.1:p.Tyr1687=
XM_011544036.1:c.2724T>C	XP_011542338.1:p.Tyr908=
XM_011544037.1:c.5061T>C	XP_011542339.1:p.Tyr1687=
XM_011544038.1:c.5061T>C	XP_011542340.1:p.Tyr1687=
XM_011544039.1:c.5061T>C	XP_011542341.1:p.Tyr1687=
XM_011544040.1:c.5061T>C	XP_011542342.1:p.Tyr1687=
XM_011544033.2:c.5061T>C	XP_011542335.1:p.Tyr1687=
XM_011544035.2:c.5061T>C	XP_011542337.1:p.Tyr1687=
XM_011544036.2:c.2724T>C	XP_011542338.1:p.Tyr908=
XM_011544037.2:c.5061T>C	XP_011542339.1:p.Tyr1687=
XM_011544039.2:c.5061T>C	XP_011542341.1:p.Tyr1687=
XM_017000150.1:c.5061T>C	XP_016855639.1:p.Tyr1687=
XM_017000151.1:c.5061T>C	XP_016855640.1:p.Tyr1687=
XR_001736946.2:n.5243T>C
XR_001736947.1:n.5243T>C
XR_001736948.1:n.5243T>C
XR_002959252.1:n.5243T>C
NM_000081.4:c.5061T>C MANE Select	NP_000072.2:p.Tyr1687=