Canonical Allele Identifier: CA1465521

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235715372G>A , CM000663.2:g.235715372G>A	GRCh38
NC_000001.10:g.235878672G>A , CM000663.1:g.235878672G>A	GRCh37
NC_000001.9:g.233945295G>A	NCBI36
NG_007397.1:g.173269C>T , LRG_143:g.173269C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.9628-15C>T MANE Select	NP_000072.2:n.9628-15C>T
ENST00000389793.7:c.9628-15C>T MANE Select	ENSP00000374443.2:n.9628-15C>T
NM_000081.3:c.9628-15C>T , LRG_143t1:c.9628-15C>T	NP_000072.2:n.9628-15C>T
NM_001301365.1:c.9628-15C>T , LRG_143t2:c.9628-15C>T	NP_001288294.1:n.9628-15C>T
ENST00000389793.6:c.9628-15C>T	ENSP00000374443.2:n.9628-15C>T
ENST00000389794.7:c.*5052-15C>T	ENSP00000374444.4:n.*5052-15C>T
ENST00000461526.2:c.5156-15C>T	ENSP00000513165.1:n.5156-15C>T
ENST00000473037.5:n.4618-15C>T
ENST00000475277.1:n.494-15C>T
ENST00000475277.2:c.1723-15C>T	ENSP00000513164.1:n.1723-15C>T
ENST00000697178.1:c.*5323-15C>T	ENSP00000513163.1:n.*5323-15C>T
ENST00000697235.1:c.178-15C>T	ENSP00000513202.1:n.178-15C>T
ENST00000697236.1:c.3092-15C>T	ENSP00000513203.1:n.3092-15C>T
ENST00000697237.1:c.584-15C>T
ENST00000697240.1:c.1762-15C>T	ENSP00000513205.1:n.1762-15C>T
ENST00000697241.1:c.4108-15C>T	ENSP00000513206.1:n.4108-15C>T
XM_011544031.1:c.9790-15C>T	XP_011542333.1:n.9790-15C>T
XM_011544032.1:c.9790-15C>T	XP_011542334.1:n.9790-15C>T
XM_011544033.1:c.9790-15C>T	XP_011542335.1:n.9790-15C>T
XM_011544033.2:c.9790-15C>T	XP_011542335.1:n.9790-15C>T
XM_011544034.1:c.9652-15C>T	XP_011542336.1:n.9652-15C>T
XM_011544035.1:c.9790-15C>T	XP_011542337.1:n.9790-15C>T
XM_011544035.2:c.9790-15C>T	XP_011542337.1:n.9790-15C>T
XM_011544036.1:c.7453-15C>T	XP_011542338.1:n.7453-15C>T
XM_011544036.2:c.7453-15C>T	XP_011542338.1:n.7453-15C>T
XM_017000150.1:c.9790-15C>T	XP_016855639.1:n.9790-15C>T
XR_001736947.1:n.10663-15C>T