Canonical Allele Identifier: CA39612458

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235751828A>G , CM000663.2:g.235751828A>G	GRCh38
NC_000001.10:g.235915128A>G , CM000663.1:g.235915128A>G	GRCh37
NC_000001.9:g.233981751A>G	NCBI36
NG_007397.1:g.136813T>C , LRG_143:g.136813T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.7627+177T>C MANE Select	NP_000072.2:n.7627+177T>C
ENST00000389793.7:c.7627+177T>C MANE Select	ENSP00000374443.2:n.7627+177T>C
NM_000081.3:c.7627+177T>C , LRG_143t1:c.7627+177T>C	NP_000072.2:n.7627+177T>C
NM_001301365.1:c.7627+177T>C , LRG_143t2:c.7627+177T>C	NP_001288294.1:n.7627+177T>C
ENST00000389793.6:c.7627+177T>C	ENSP00000374443.2:n.7627+177T>C
ENST00000389794.7:c.*3051+177T>C	ENSP00000374444.4:n.*3051+177T>C
ENST00000461526.2:c.2302+177T>C	ENSP00000513165.1:n.2302+177T>C
ENST00000487530.2:c.167+177T>C
ENST00000697178.1:c.*3051+177T>C	ENSP00000513163.1:n.*3051+177T>C
ENST00000697236.1:c.1336+177T>C	ENSP00000513203.1:n.1336+177T>C
ENST00000697241.1:c.2107+177T>C	ENSP00000513206.1:n.2107+177T>C
XM_011544031.1:c.7627+177T>C	XP_011542333.1:n.7627+177T>C
XM_011544032.1:c.7627+177T>C	XP_011542334.1:n.7627+177T>C
XM_011544033.1:c.7627+177T>C	XP_011542335.1:n.7627+177T>C
XM_011544033.2:c.7627+177T>C	XP_011542335.1:n.7627+177T>C
XM_011544034.1:c.7489+177T>C	XP_011542336.1:n.7489+177T>C
XM_011544035.1:c.7627+177T>C	XP_011542337.1:n.7627+177T>C
XM_011544035.2:c.7627+177T>C	XP_011542337.1:n.7627+177T>C
XM_011544036.1:c.5290+177T>C	XP_011542338.1:n.5290+177T>C
XM_011544036.2:c.5290+177T>C	XP_011542338.1:n.5290+177T>C
XM_011544037.1:c.7627+177T>C	XP_011542339.1:n.7627+177T>C
XM_011544037.2:c.7627+177T>C	XP_011542339.1:n.7627+177T>C
XM_011544038.1:c.7627+177T>C	XP_011542340.1:n.7627+177T>C
XM_011544039.1:c.7627+177T>C	XP_011542341.1:n.7627+177T>C
XM_011544039.2:c.7627+177T>C	XP_011542341.1:n.7627+177T>C
XM_017000150.1:c.7627+177T>C	XP_016855639.1:n.7627+177T>C
XR_001736946.2:n.7809+177T>C
XR_001736947.1:n.7809+177T>C
XR_001736948.1:n.7411+3650T>C