Canonical Allele Identifier: CA1465865

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235734626A>G , CM000663.2:g.235734626A>G	GRCh38
NC_000001.10:g.235897926A>G , CM000663.1:g.235897926A>G	GRCh37
NC_000001.9:g.233964549A>G	NCBI36
NG_007397.1:g.154015T>C , LRG_143:g.154015T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.3920T>C	ENSP00000513165.1:n.3920T>C
ENST00000475277.2:c.487T>C	ENSP00000513164.1:p.Leu163=
ENST00000697178.1:c.*3816T>C	ENSP00000513163.1:n.*3816T>C
ENST00000697236.1:c.2101T>C	ENSP00000513203.1:p.Leu701=
ENST00000697240.1:c.526T>C	ENSP00000513205.1:p.Leu176=
ENST00000697241.1:c.2872T>C	ENSP00000513206.1:p.Leu958=
ENST00000389793.7:c.8392T>C MANE Select	ENSP00000374443.2:p.Leu2798=
ENST00000389793.6:c.8392T>C	ENSP00000374443.2:p.Leu2798=
ENST00000389794.7:c.*3816T>C	ENSP00000374444.4:n.*3816T>C
ENST00000473037.5:n.3382T>C
NM_000081.3:c.8392T>C , LRG_143t1:c.8392T>C	NP_000072.2:p.Leu2798=
NM_001301365.1:c.8392T>C , LRG_143t2:c.8392T>C	NP_001288294.1:p.Leu2798=
XM_011544031.1:c.8554T>C	XP_011542333.1:p.Leu2852=
XM_011544032.1:c.8554T>C	XP_011542334.1:p.Leu2852=
XM_011544033.1:c.8554T>C	XP_011542335.1:p.Leu2852=
XM_011544034.1:c.8416T>C	XP_011542336.1:p.Leu2806=
XM_011544035.1:c.8554T>C	XP_011542337.1:p.Leu2852=
XM_011544036.1:c.6217T>C	XP_011542338.1:p.Leu2073=
XM_011544033.2:c.8554T>C	XP_011542335.1:p.Leu2852=
XM_011544035.2:c.8554T>C	XP_011542337.1:p.Leu2852=
XM_011544036.2:c.6217T>C	XP_011542338.1:p.Leu2073=
XM_017000150.1:c.8554T>C	XP_016855639.1:p.Leu2852=
XR_001736946.2:n.9589T>C
XR_001736947.1:n.9427T>C
NM_000081.4:c.8392T>C MANE Select	NP_000072.2:p.Leu2798=