Canonical Allele Identifier: CA2651136308

Gene: LYST

Linked Data

• gnomAD v4: 1-235766044-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235766044A>G , CM000663.2:g.235766044A>G	GRCh38
NC_000001.10:g.235929344A>G , CM000663.1:g.235929344A>G	GRCh37
NC_000001.9:g.233995967A>G	NCBI36
NG_007397.1:g.122597T>C , LRG_143:g.122597T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461526.2:c.796+35T>C	ENSP00000513165.1:n.796+35T>C
ENST00000697178.1:c.*1545+35T>C	ENSP00000513163.1:n.*1545+35T>C
ENST00000697180.1:c.626+35T>C
ENST00000697241.1:c.553+35T>C	ENSP00000513206.1:n.553+35T>C
ENST00000389793.7:c.6121+35T>C MANE Select	ENSP00000374443.2:n.6121+35T>C
ENST00000389793.6:c.6121+35T>C	ENSP00000374443.2:n.6121+35T>C
ENST00000389794.7:c.*1545+35T>C	ENSP00000374444.4:n.*1545+35T>C
ENST00000489585.5:n.6512+195T>C
NM_000081.3:c.6121+35T>C , LRG_143t1:c.6121+35T>C	NP_000072.2:n.6121+35T>C
NM_001301365.1:c.6121+35T>C , LRG_143t2:c.6121+35T>C	NP_001288294.1:n.6121+35T>C
XM_011544031.1:c.6121+35T>C	XP_011542333.1:n.6121+35T>C
XM_011544032.1:c.6121+35T>C	XP_011542334.1:n.6121+35T>C
XM_011544033.1:c.6121+35T>C	XP_011542335.1:n.6121+35T>C
XM_011544034.1:c.5983+35T>C	XP_011542336.1:n.5983+35T>C
XM_011544035.1:c.6121+35T>C	XP_011542337.1:n.6121+35T>C
XM_011544036.1:c.3784+35T>C	XP_011542338.1:n.3784+35T>C
XM_011544037.1:c.6121+35T>C	XP_011542339.1:n.6121+35T>C
XM_011544038.1:c.6121+35T>C	XP_011542340.1:n.6121+35T>C
XM_011544039.1:c.6121+35T>C	XP_011542341.1:n.6121+35T>C
XM_011544040.1:c.6030+35T>C	XP_011542342.1:n.6030+35T>C
XM_011544033.2:c.6121+35T>C	XP_011542335.1:n.6121+35T>C
XM_011544035.2:c.6121+35T>C	XP_011542337.1:n.6121+35T>C
XM_011544036.2:c.3784+35T>C	XP_011542338.1:n.3784+35T>C
XM_011544037.2:c.6121+35T>C	XP_011542339.1:n.6121+35T>C
XM_011544039.2:c.6121+35T>C	XP_011542341.1:n.6121+35T>C
XM_017000150.1:c.6121+35T>C	XP_016855639.1:n.6121+35T>C
XM_017000151.1:c.5892+35T>C	XP_016855640.1:n.5892+35T>C
XR_001736946.2:n.6303+35T>C
XR_001736947.1:n.6303+35T>C
XR_001736948.1:n.6303+35T>C
XR_002959252.1:n.6212+35T>C
NM_000081.4:c.6121+35T>C MANE Select	NP_000072.2:n.6121+35T>C