Canonical Allele Identifier: CA344934695

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235709139C>A , CM000663.2:g.235709139C>A	GRCh38
NC_000001.10:g.235872439C>A , CM000663.1:g.235872439C>A	GRCh37
NC_000001.9:g.233939062C>A	NCBI36
NG_007397.1:g.179502G>T , LRG_143:g.179502G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.10095G>T MANE Select	NP_000072.2:p.Lys3365Asn
ENST00000389793.7:c.10095G>T MANE Select	ENSP00000374443.2:p.Lys3365Asn
NM_000081.3:c.10095G>T , LRG_143t1:c.10095G>T	NP_000072.2:p.Lys3365Asn
NM_001301365.1:c.10095G>T , LRG_143t2:c.10095G>T	NP_001288294.1:p.Lys3365Asn
ENST00000389793.6:c.10095G>T	ENSP00000374443.2:p.Lys3365Asn
ENST00000389794.7:c.*5519G>T	ENSP00000374444.4:n.*5519G>T
ENST00000462376.1:n.514G>T
ENST00000462376.2:n.1505G>T
ENST00000473037.5:n.5085G>T
ENST00000697178.1:c.*5790G>T	ENSP00000513163.1:n.*5790G>T
ENST00000697179.1:n.2804G>T
ENST00000697235.1:c.645G>T	ENSP00000513202.1:p.Lys215Asn
ENST00000697236.1:c.3559G>T	ENSP00000513203.1:n.3559G>T
ENST00000697237.1:c.806G>T
ENST00000697240.1:c.2229G>T	ENSP00000513205.1:p.Lys743Asn
XM_011544031.1:c.10257G>T	XP_011542333.1:p.Lys3419Asn
XM_011544032.1:c.10257G>T	XP_011542334.1:p.Lys3419Asn
XM_011544033.1:c.10257G>T	XP_011542335.1:p.Lys3419Asn
XM_011544033.2:c.10257G>T	XP_011542335.1:p.Lys3419Asn
XM_011544034.1:c.10119G>T	XP_011542336.1:p.Lys3373Asn
XM_011544036.1:c.7920G>T	XP_011542338.1:p.Lys2640Asn
XM_011544036.2:c.7920G>T	XP_011542338.1:p.Lys2640Asn
XM_017000150.1:c.10257G>T	XP_016855639.1:p.Lys3419Asn