Canonical Allele Identifier: CA423758781

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235687006A>G , CM000663.2:g.235687006A>G	GRCh38
NC_000001.10:g.235850306A>G , CM000663.1:g.235850306A>G	GRCh37
NC_000001.9:g.233916929A>G	NCBI36
NG_007397.1:g.201635T>C , LRG_143:g.201635T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.2153T>C
ENST00000697178.1:c.*6438T>C	ENSP00000513163.1:n.*6438T>C
ENST00000697235.1:c.1293T>C	ENSP00000513202.1:p.Phe431=
ENST00000697236.1:c.4207T>C	ENSP00000513203.1:n.4207T>C
ENST00000697237.1:c.1454T>C
ENST00000697239.1:n.137T>C
ENST00000697240.1:c.2877T>C	ENSP00000513205.1:p.Phe959=
ENST00000389793.7:c.10743T>C MANE Select	ENSP00000374443.2:p.Phe3581=
ENST00000389793.6:c.10743T>C	ENSP00000374443.2:p.Phe3581=
ENST00000389794.7:c.*6167T>C	ENSP00000374444.4:n.*6167T>C
ENST00000473037.5:n.5733T>C
NM_000081.3:c.10743T>C , LRG_143t1:c.10743T>C	NP_000072.2:p.Phe3581=
NM_001301365.1:c.10743T>C , LRG_143t2:c.10743T>C	NP_001288294.1:p.Phe3581=
XM_011544031.1:c.10905T>C	XP_011542333.1:p.Phe3635=
XM_011544032.1:c.10905T>C	XP_011542334.1:p.Phe3635=
XM_011544033.1:c.10905T>C	XP_011542335.1:p.Phe3635=
XM_011544034.1:c.10767T>C	XP_011542336.1:p.Phe3589=
XM_011544036.1:c.8568T>C	XP_011542338.1:p.Phe2856=
XM_011544033.2:c.10905T>C	XP_011542335.1:p.Phe3635=
XM_011544036.2:c.8568T>C	XP_011542338.1:p.Phe2856=
XM_017000150.1:c.10674T>C	XP_016855639.1:p.Phe3558=
NM_000081.4:c.10743T>C MANE Select	NP_000072.2:p.Phe3581=