Canonical Allele Identifier: CA344932506
Community Standard Title: NM_000081.4(LYST):c.10153G>T (p.Gly3385Ter)
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235702968C>A , CM000663.2:g.235702968C>A GRCh38
NC_000001.10:g.235866268C>A , CM000663.1:g.235866268C>A GRCh37
NC_000001.9:g.233932891C>A NCBI36
NG_007397.1:g.185673G>T , LRG_143:g.185673G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000081.4:c.10153G>T MANE Select NP_000072.2:p.Gly3385Ter
ENST00000389793.7:c.10153G>T MANE Select ENSP00000374443.2:p.Gly3385Ter
NM_000081.3:c.10153G>T , LRG_143t1:c.10153G>T NP_000072.2:p.Gly3385Ter
NM_001301365.1:c.10153G>T , LRG_143t2:c.10153G>T NP_001288294.1:p.Gly3385Ter
ENST00000389793.6:c.10153G>T ENSP00000374443.2:p.Gly3385Ter
ENST00000389794.7:c.*5577G>T ENSP00000374444.4:n.*5577G>T
ENST00000462376.2:n.1563G>T
ENST00000473037.5:n.5143G>T
ENST00000697178.1:c.*5848G>T ENSP00000513163.1:n.*5848G>T
ENST00000697179.1:n.2862G>T
ENST00000697235.1:c.703G>T ENSP00000513202.1:p.Gly235Ter
ENST00000697236.1:c.3617G>T ENSP00000513203.1:n.3617G>T
ENST00000697237.1:c.864G>T
ENST00000697240.1:c.2287G>T ENSP00000513205.1:p.Gly763Ter
XM_011544031.1:c.10315G>T XP_011542333.1:p.Gly3439Ter
XM_011544032.1:c.10315G>T XP_011542334.1:p.Gly3439Ter
XM_011544033.1:c.10315G>T XP_011542335.1:p.Gly3439Ter
XM_011544033.2:c.10315G>T XP_011542335.1:p.Gly3439Ter
XM_011544034.1:c.10177G>T XP_011542336.1:p.Gly3393Ter
XM_011544036.1:c.7978G>T XP_011542338.1:p.Gly2660Ter
XM_011544036.2:c.7978G>T XP_011542338.1:p.Gly2660Ter
XM_017000150.1:c.10306-5696G>T XP_016855639.1:n.10306-5696G>T