Canonical Allele Identifier: CA1465604

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235720883T>C , CM000663.2:g.235720883T>C	GRCh38
NC_000001.10:g.235884183T>C , CM000663.1:g.235884183T>C	GRCh37
NC_000001.9:g.233950806T>C	NCBI36
NG_007397.1:g.167758A>G , LRG_143:g.167758A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9338A>G MANE Select	NP_000072.2:p.Asn3113Ser
ENST00000389793.7:c.9338A>G MANE Select	ENSP00000374443.2:p.Asn3113Ser
NM_000081.3:c.9338A>G , LRG_143t1:c.9338A>G	NP_000072.2:p.Asn3113Ser
NM_001301365.1:c.9338A>G , LRG_143t2:c.9338A>G	NP_001288294.1:p.Asn3113Ser
ENST00000389793.6:c.9338A>G	ENSP00000374443.2:p.Asn3113Ser
ENST00000389794.7:c.*4762A>G	ENSP00000374444.4:n.*4762A>G
ENST00000461526.2:c.4866A>G	ENSP00000513165.1:n.4866A>G
ENST00000473037.5:n.4328A>G
ENST00000475277.1:n.204A>G
ENST00000475277.2:c.1433A>G	ENSP00000513164.1:p.Asn478Ser
ENST00000697178.1:c.*4762A>G	ENSP00000513163.1:n.*4762A>G
ENST00000697235.1:c.8A>G	ENSP00000513202.1:p.Asn3Ser
ENST00000697236.1:c.3024+3145A>G	ENSP00000513203.1:n.3024+3145A>G
ENST00000697237.1:c.294A>G
ENST00000697240.1:c.1472A>G	ENSP00000513205.1:p.Asn491Ser
ENST00000697241.1:c.3818A>G	ENSP00000513206.1:p.Asn1273Ser
XM_011544031.1:c.9500A>G	XP_011542333.1:p.Asn3167Ser
XM_011544032.1:c.9500A>G	XP_011542334.1:p.Asn3167Ser
XM_011544033.1:c.9500A>G	XP_011542335.1:p.Asn3167Ser
XM_011544033.2:c.9500A>G	XP_011542335.1:p.Asn3167Ser
XM_011544034.1:c.9362A>G	XP_011542336.1:p.Asn3121Ser
XM_011544035.1:c.9500A>G	XP_011542337.1:p.Asn3167Ser
XM_011544035.2:c.9500A>G	XP_011542337.1:p.Asn3167Ser
XM_011544036.1:c.7163A>G	XP_011542338.1:p.Asn2388Ser
XM_011544036.2:c.7163A>G	XP_011542338.1:p.Asn2388Ser
XM_017000150.1:c.9500A>G	XP_016855639.1:p.Asn3167Ser
XR_001736947.1:n.10373A>G