Canonical Allele Identifier: CA344926857

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235693450G>T , CM000663.2:g.235693450G>T	GRCh38
NC_000001.10:g.235856750G>T , CM000663.1:g.235856750G>T	GRCh37
NC_000001.9:g.233923373G>T	NCBI36
NG_007397.1:g.195191C>A , LRG_143:g.195191C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.10601C>A MANE Select	NP_000072.2:p.Ser3534Ter
ENST00000389793.7:c.10601C>A MANE Select	ENSP00000374443.2:p.Ser3534Ter
NM_000081.3:c.10601C>A , LRG_143t1:c.10601C>A	NP_000072.2:p.Ser3534Ter
NM_001301365.1:c.10601C>A , LRG_143t2:c.10601C>A	NP_001288294.1:p.Ser3534Ter
ENST00000389793.6:c.10601C>A	ENSP00000374443.2:p.Ser3534Ter
ENST00000389794.7:c.*6025C>A	ENSP00000374444.4:n.*6025C>A
ENST00000462376.2:n.2011C>A
ENST00000473037.5:n.5591C>A
ENST00000697178.1:c.*6296C>A	ENSP00000513163.1:n.*6296C>A
ENST00000697235.1:c.1151C>A	ENSP00000513202.1:p.Ser384Ter
ENST00000697236.1:c.4065C>A	ENSP00000513203.1:n.4065C>A
ENST00000697237.1:c.1312C>A
ENST00000697240.1:c.2735C>A	ENSP00000513205.1:p.Ser912Ter
XM_011544031.1:c.10763C>A	XP_011542333.1:p.Ser3588Ter
XM_011544032.1:c.10763C>A	XP_011542334.1:p.Ser3588Ter
XM_011544033.1:c.10763C>A	XP_011542335.1:p.Ser3588Ter
XM_011544033.2:c.10763C>A	XP_011542335.1:p.Ser3588Ter
XM_011544034.1:c.10625C>A	XP_011542336.1:p.Ser3542Ter
XM_011544036.1:c.8426C>A	XP_011542338.1:p.Ser2809Ter
XM_011544036.2:c.8426C>A	XP_011542338.1:p.Ser2809Ter
XM_017000150.1:c.10532C>A	XP_016855639.1:p.Ser3511Ter