Canonical Allele Identifier: CA10610427

Gene: LYST

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235662049C>G , CM000663.2:g.235662049C>G	GRCh38
NC_000001.10:g.235825349C>G , CM000663.1:g.235825349C>G	GRCh37
NC_000001.9:g.233891972C>G	NCBI36
NG_007397.1:g.226592G>C , LRG_143:g.226592G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462376.2:n.4116G>C
ENST00000697178.1:c.*8283G>C	ENSP00000513163.1:n.*8283G>C
ENST00000697235.1:c.2847G>C	ENSP00000513202.1:n.2847G>C
ENST00000697236.1:c.5761G>C	ENSP00000513203.1:n.5761G>C
ENST00000697237.1:c.3008G>C
ENST00000389793.7:c.*891G>C MANE Select	ENSP00000374443.2:n.*891G>C
ENST00000389793.6:c.*891G>C	ENSP00000374443.2:n.*891G>C
ENST00000389794.7:c.*7721G>C	ENSP00000374444.4:n.*7721G>C
ENST00000473037.5:n.7287G>C
NM_000081.3:c.*891G>C , LRG_143t1:c.*891G>C	NP_000072.2:n.*891G>C
NM_001301365.1:c.*891G>C , LRG_143t2:c.*891G>C	NP_001288294.1:n.*891G>C
XM_011544031.1:c.*891G>C	XP_011542333.1:n.*891G>C
XM_011544032.1:c.*891G>C	XP_011542334.1:n.*891G>C
XM_011544033.1:c.*891G>C	XP_011542335.1:n.*891G>C
XM_011544034.1:c.*891G>C	XP_011542336.1:n.*891G>C
XM_011544036.1:c.*891G>C	XP_011542338.1:n.*891G>C
XM_011544033.2:c.*891G>C	XP_011542335.1:n.*891G>C
XM_011544036.2:c.*891G>C	XP_011542338.1:n.*891G>C
XM_017000150.1:c.*891G>C	XP_016855639.1:n.*891G>C
NM_000081.4:c.*891G>C MANE Select	NP_000072.2:n.*891G>C