Canonical Allele Identifier: CA1465690

Gene: LYST

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235729670A>G , CM000663.2:g.235729670A>G	GRCh38
NC_000001.10:g.235892970A>G , CM000663.1:g.235892970A>G	GRCh37
NC_000001.9:g.233959593A>G	NCBI36
NG_007397.1:g.158971T>C , LRG_143:g.158971T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.4573-13T>C	ENSP00000513165.1:n.4573-13T>C
ENST00000475277.2:c.1140-13T>C	ENSP00000513164.1:n.1140-13T>C
ENST00000697178.1:c.*4469-13T>C	ENSP00000513163.1:n.*4469-13T>C
ENST00000697236.1:c.2754-13T>C	ENSP00000513203.1:n.2754-13T>C
ENST00000697240.1:c.1179-13T>C	ENSP00000513205.1:n.1179-13T>C
ENST00000697241.1:c.3525-13T>C	ENSP00000513206.1:n.3525-13T>C
ENST00000389793.7:c.9045-13T>C MANE Select	ENSP00000374443.2:n.9045-13T>C
ENST00000389793.6:c.9045-13T>C	ENSP00000374443.2:n.9045-13T>C
ENST00000389794.7:c.*4469-13T>C	ENSP00000374444.4:n.*4469-13T>C
ENST00000473037.5:n.4035-13T>C
NM_000081.3:c.9045-13T>C , LRG_143t1:c.9045-13T>C	NP_000072.2:n.9045-13T>C
NM_001301365.1:c.9045-13T>C , LRG_143t2:c.9045-13T>C	NP_001288294.1:n.9045-13T>C
XM_011544031.1:c.9207-13T>C	XP_011542333.1:n.9207-13T>C
XM_011544032.1:c.9207-13T>C	XP_011542334.1:n.9207-13T>C
XM_011544033.1:c.9207-13T>C	XP_011542335.1:n.9207-13T>C
XM_011544034.1:c.9069-13T>C	XP_011542336.1:n.9069-13T>C
XM_011544035.1:c.9207-13T>C	XP_011542337.1:n.9207-13T>C
XM_011544036.1:c.6870-13T>C	XP_011542338.1:n.6870-13T>C
XM_011544033.2:c.9207-13T>C	XP_011542335.1:n.9207-13T>C
XM_011544035.2:c.9207-13T>C	XP_011542337.1:n.9207-13T>C
XM_011544036.2:c.6870-13T>C	XP_011542338.1:n.6870-13T>C
XM_017000150.1:c.9207-13T>C	XP_016855639.1:n.9207-13T>C
XR_001736947.1:n.10080-13T>C
NM_000081.4:c.9045-13T>C MANE Select	NP_000072.2:n.9045-13T>C