Canonical Allele Identifier: CA10609573

Gene: LYST

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235866885C>G , CM000663.2:g.235866885C>G	GRCh38
NC_000001.10:g.236030185C>G , CM000663.1:g.236030185C>G	GRCh37
NC_000001.9:g.234096808C>G	NCBI36
NG_007397.1:g.21756G>C , LRG_143:g.21756G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697178.1:c.-98+16302G>C	ENSP00000513163.1:n.-98+16302G>C
ENST00000697181.1:c.-98+16302G>C	ENSP00000513168.1:n.-98+16302G>C
ENST00000697182.1:c.-98+16302G>C	ENSP00000513169.1:n.-98+16302G>C
ENST00000697183.1:c.-140G>C	ENSP00000513170.1:n.-140G>C
ENST00000697184.1:c.-140G>C	ENSP00000513171.1:n.-140G>C
ENST00000697242.1:c.-140G>C	ENSP00000513207.1:n.-140G>C
ENST00000389793.7:c.-140G>C MANE Select	ENSP00000374443.2:n.-140G>C
ENST00000389793.6:c.-140G>C	ENSP00000374443.2:n.-140G>C
ENST00000389794.7:c.-140G>C	ENSP00000374444.4:n.-140G>C
ENST00000465349.5:n.454+16302G>C
ENST00000468107.5:n.430+16302G>C
ENST00000489585.5:n.454+16302G>C
NM_000081.3:c.-140G>C , LRG_143t1:c.-140G>C	NP_000072.2:n.-140G>C
NM_001301365.1:c.-98+16302G>C , LRG_143t2:c.-98+16302G>C	NP_001288294.1:n.-98+16302G>C
NR_102436.2:n.522+16302G>C
XM_011544031.1:c.-140G>C	XP_011542333.1:n.-140G>C
XM_011544032.1:c.-98+16302G>C	XP_011542334.1:n.-98+16302G>C
XM_011544034.1:c.-140G>C	XP_011542336.1:n.-140G>C
XM_011544035.1:c.-140G>C	XP_011542337.1:n.-140G>C
XM_011544037.1:c.-140G>C	XP_011542339.1:n.-140G>C
XM_011544038.1:c.-140G>C	XP_011542340.1:n.-140G>C
XM_011544039.1:c.-140G>C	XP_011542341.1:n.-140G>C
XM_011544040.1:c.-140G>C	XP_011542342.1:n.-140G>C
XM_011544035.2:c.-140G>C	XP_011542337.1:n.-140G>C
XM_011544037.2:c.-140G>C	XP_011542339.1:n.-140G>C
XM_011544039.2:c.-140G>C	XP_011542341.1:n.-140G>C
XM_017000150.1:c.-140G>C	XP_016855639.1:n.-140G>C
XM_017000151.1:c.-140G>C	XP_016855640.1:n.-140G>C
XR_001736946.2:n.43G>C
XR_001736947.1:n.43G>C
XR_001736948.1:n.43G>C
XR_002959252.1:n.43G>C
NM_000081.4:c.-140G>C MANE Select	NP_000072.2:n.-140G>C
NR_102436.3:n.527+16302G>C