Canonical Allele Identifier: CA1465729

Gene: LYST

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235731066A>C , CM000663.2:g.235731066A>C	GRCh38
NC_000001.10:g.235894366A>C , CM000663.1:g.235894366A>C	GRCh37
NC_000001.9:g.233960989A>C	NCBI36
NG_007397.1:g.157575T>G , LRG_143:g.157575T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.4441T>G	ENSP00000513165.1:n.4441T>G
ENST00000475277.2:c.1008T>G	ENSP00000513164.1:p.Asn336Lys
ENST00000697178.1:c.*4337T>G	ENSP00000513163.1:n.*4337T>G
ENST00000697236.1:c.2622T>G	ENSP00000513203.1:p.Asn874Lys
ENST00000697240.1:c.1047T>G	ENSP00000513205.1:p.Asn349Lys
ENST00000697241.1:c.3393T>G	ENSP00000513206.1:p.Asn1131Lys
ENST00000389793.7:c.8913T>G MANE Select	ENSP00000374443.2:p.Asn2971Lys
ENST00000389793.6:c.8913T>G	ENSP00000374443.2:p.Asn2971Lys
ENST00000389794.7:c.*4337T>G	ENSP00000374444.4:n.*4337T>G
ENST00000473037.5:n.3903T>G
NM_000081.3:c.8913T>G , LRG_143t1:c.8913T>G	NP_000072.2:p.Asn2971Lys
NM_001301365.1:c.8913T>G , LRG_143t2:c.8913T>G	NP_001288294.1:p.Asn2971Lys
XM_011544031.1:c.9075T>G	XP_011542333.1:p.Asn3025Lys
XM_011544032.1:c.9075T>G	XP_011542334.1:p.Asn3025Lys
XM_011544033.1:c.9075T>G	XP_011542335.1:p.Asn3025Lys
XM_011544034.1:c.8937T>G	XP_011542336.1:p.Asn2979Lys
XM_011544035.1:c.9075T>G	XP_011542337.1:p.Asn3025Lys
XM_011544036.1:c.6738T>G	XP_011542338.1:p.Asn2246Lys
XM_011544033.2:c.9075T>G	XP_011542335.1:p.Asn3025Lys
XM_011544035.2:c.9075T>G	XP_011542337.1:p.Asn3025Lys
XM_011544036.2:c.6738T>G	XP_011542338.1:p.Asn2246Lys
XM_017000150.1:c.9075T>G	XP_016855639.1:p.Asn3025Lys
XR_001736947.1:n.9948T>G
NM_000081.4:c.8913T>G MANE Select	NP_000072.2:p.Asn2971Lys