Canonical Allele Identifier: CA344920672

Gene: LYST

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235733860C>T , CM000663.2:g.235733860C>T	GRCh38
NC_000001.10:g.235897160C>T , CM000663.1:g.235897160C>T	GRCh37
NC_000001.9:g.233963783C>T	NCBI36
NG_007397.1:g.154781G>A , LRG_143:g.154781G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461526.2:c.4110G>A	ENSP00000513165.1:n.4110G>A
ENST00000475277.2:c.677G>A	ENSP00000513164.1:p.Trp226Ter
ENST00000697178.1:c.*4006G>A	ENSP00000513163.1:n.*4006G>A
ENST00000697236.1:c.2291G>A	ENSP00000513203.1:p.Trp764Ter
ENST00000697240.1:c.716G>A	ENSP00000513205.1:p.Trp239Ter
ENST00000697241.1:c.3062G>A	ENSP00000513206.1:p.Trp1021Ter
ENST00000389793.7:c.8582G>A MANE Select	ENSP00000374443.2:p.Trp2861Ter
ENST00000389793.6:c.8582G>A	ENSP00000374443.2:p.Trp2861Ter
ENST00000389794.7:c.*4006G>A	ENSP00000374444.4:n.*4006G>A
ENST00000473037.5:n.3572G>A
NM_000081.3:c.8582G>A , LRG_143t1:c.8582G>A	NP_000072.2:p.Trp2861Ter
NM_001301365.1:c.8582G>A , LRG_143t2:c.8582G>A	NP_001288294.1:p.Trp2861Ter
XM_011544031.1:c.8744G>A	XP_011542333.1:p.Trp2915Ter
XM_011544032.1:c.8744G>A	XP_011542334.1:p.Trp2915Ter
XM_011544033.1:c.8744G>A	XP_011542335.1:p.Trp2915Ter
XM_011544034.1:c.8606G>A	XP_011542336.1:p.Trp2869Ter
XM_011544035.1:c.8744G>A	XP_011542337.1:p.Trp2915Ter
XM_011544036.1:c.6407G>A	XP_011542338.1:p.Trp2136Ter
XM_011544033.2:c.8744G>A	XP_011542335.1:p.Trp2915Ter
XM_011544035.2:c.8744G>A	XP_011542337.1:p.Trp2915Ter
XM_011544036.2:c.6407G>A	XP_011542338.1:p.Trp2136Ter
XM_017000150.1:c.8744G>A	XP_016855639.1:p.Trp2915Ter
XR_001736947.1:n.9617G>A
NM_000081.4:c.8582G>A MANE Select	NP_000072.2:p.Trp2861Ter