Canonical Allele Identifier: CA1465277

Gene: LYST

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235677597G>C , CM000663.2:g.235677597G>C	GRCh38
NC_000001.10:g.235840897G>C , CM000663.1:g.235840897G>C	GRCh37
NC_000001.9:g.233907520G>C	NCBI36
NG_007397.1:g.211044C>G , LRG_143:g.211044C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000081.4:c.10823C>G MANE Select	NP_000072.2:p.Thr3608Ser
ENST00000389793.7:c.10823C>G MANE Select	ENSP00000374443.2:p.Thr3608Ser
NM_000081.3:c.10823C>G , LRG_143t1:c.10823C>G	NP_000072.2:p.Thr3608Ser
NM_001301365.1:c.10823C>G , LRG_143t2:c.10823C>G	NP_001288294.1:p.Thr3608Ser
ENST00000389793.6:c.10823C>G	ENSP00000374443.2:p.Thr3608Ser
ENST00000389794.7:c.*6247C>G	ENSP00000374444.4:n.*6247C>G
ENST00000462376.2:n.2233C>G
ENST00000473037.5:n.5813C>G
ENST00000697178.1:c.*6518C>G	ENSP00000513163.1:n.*6518C>G
ENST00000697235.1:c.1373C>G	ENSP00000513202.1:p.Thr458Ser
ENST00000697236.1:c.4287C>G	ENSP00000513203.1:n.4287C>G
ENST00000697237.1:c.1534C>G
ENST00000697239.1:n.217C>G
ENST00000697240.1:c.2957C>G	ENSP00000513205.1:p.Thr986Ser
XM_011544031.1:c.10985C>G	XP_011542333.1:p.Thr3662Ser
XM_011544032.1:c.10985C>G	XP_011542334.1:p.Thr3662Ser
XM_011544033.1:c.10985C>G	XP_011542335.1:p.Thr3662Ser
XM_011544033.2:c.10985C>G	XP_011542335.1:p.Thr3662Ser
XM_011544034.1:c.10847C>G	XP_011542336.1:p.Thr3616Ser
XM_011544036.1:c.8648C>G	XP_011542338.1:p.Thr2883Ser
XM_011544036.2:c.8648C>G	XP_011542338.1:p.Thr2883Ser
XM_017000150.1:c.10754C>G	XP_016855639.1:p.Thr3585Ser