Canonical Allele Identifier: CA1465660

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235728061T>C , CM000663.2:g.235728061T>C	GRCh38
NC_000001.10:g.235891361T>C , CM000663.1:g.235891361T>C	GRCh37
NC_000001.9:g.233957984T>C	NCBI36
NG_007397.1:g.160580A>G , LRG_143:g.160580A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9162+15A>G MANE Select	NP_000072.2:n.9162+15A>G
ENST00000389793.7:c.9162+15A>G MANE Select	ENSP00000374443.2:n.9162+15A>G
NM_000081.3:c.9162+15A>G , LRG_143t1:c.9162+15A>G	NP_000072.2:n.9162+15A>G
NM_001301365.1:c.9162+15A>G , LRG_143t2:c.9162+15A>G	NP_001288294.1:n.9162+15A>G
ENST00000389793.6:c.9162+15A>G	ENSP00000374443.2:n.9162+15A>G
ENST00000389794.7:c.*4586+15A>G	ENSP00000374444.4:n.*4586+15A>G
ENST00000461526.2:c.4690+15A>G	ENSP00000513165.1:n.4690+15A>G
ENST00000473037.5:n.4152+15A>G
ENST00000475277.1:n.28+15A>G
ENST00000475277.2:c.1257+15A>G	ENSP00000513164.1:n.1257+15A>G
ENST00000697178.1:c.*4586+15A>G	ENSP00000513163.1:n.*4586+15A>G
ENST00000697236.1:c.2871+15A>G	ENSP00000513203.1:n.2871+15A>G
ENST00000697237.1:c.118+15A>G
ENST00000697240.1:c.1296+15A>G	ENSP00000513205.1:n.1296+15A>G
ENST00000697241.1:c.3642+15A>G	ENSP00000513206.1:n.3642+15A>G
XM_011544031.1:c.9324+15A>G	XP_011542333.1:n.9324+15A>G
XM_011544032.1:c.9324+15A>G	XP_011542334.1:n.9324+15A>G
XM_011544033.1:c.9324+15A>G	XP_011542335.1:n.9324+15A>G
XM_011544033.2:c.9324+15A>G	XP_011542335.1:n.9324+15A>G
XM_011544034.1:c.9186+15A>G	XP_011542336.1:n.9186+15A>G
XM_011544035.1:c.9324+15A>G	XP_011542337.1:n.9324+15A>G
XM_011544035.2:c.9324+15A>G	XP_011542337.1:n.9324+15A>G
XM_011544036.1:c.6987+15A>G	XP_011542338.1:n.6987+15A>G
XM_011544036.2:c.6987+15A>G	XP_011542338.1:n.6987+15A>G
XM_017000150.1:c.9324+15A>G	XP_016855639.1:n.9324+15A>G
XR_001736947.1:n.10197+15A>G