Canonical Allele Identifier: CA344882
Gene: LYST HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235724114_235724115insACTGAAAGAA , CM000663.2:g.235724114_235724115insACTGAAAGAA GRCh38
NC_000001.10:g.235887414_235887415insACTGAAAGAA , CM000663.1:g.235887414_235887415insACTGAAAGAA GRCh37
NC_000001.9:g.233954037_233954038insACTGAAAGAA NCBI36
NG_007397.1:g.164526_164527insTTCTTTCAGT , LRG_143:g.164526_164527insTTCTTTCAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000461526.2:c.4756_4757insTTCTTTCAGT ENSP00000513165.1:n.4756_4757insTTCTTTCAGT
ENST00000475277.2:c.1323_1324insTTCTTTCAGT ENSP00000513164.1:p.Lys442PhefsTer4
ENST00000697178.1:c.*4652_*4653insTTCTTTCAGT ENSP00000513163.1:n.*4652_*4653insTTCTTTCAGT
ENST00000697236.1:c.2937_2938insTTCTTTCAGT ENSP00000513203.1:p.Lys980PhefsTer4
ENST00000697237.1:c.184_185insTTCTTTCAGT
ENST00000697240.1:c.1362_1363insTTCTTTCAGT ENSP00000513205.1:p.Lys455PhefsTer4
ENST00000697241.1:c.3708_3709insTTCTTTCAGT ENSP00000513206.1:p.Lys1237PhefsTer4
ENST00000389793.7:c.9228_9229insTTCTTTCAGT MANE Select ENSP00000374443.2:p.Lys3077PhefsTer4
ENST00000389793.6:c.9228_9229insTTCTTTCAGT ENSP00000374443.2:p.Lys3077PhefsTer4
ENST00000389794.7:c.*4652_*4653insTTCTTTCAGT ENSP00000374444.4:n.*4652_*4653insTTCTTTCAGT
ENST00000473037.5:n.4218_4219insTTCTTTCAGT
ENST00000475277.1:n.94_95insTTCTTTCAGT
NM_000081.3:c.9228_9229insTTCTTTCAGT , LRG_143t1:c.9228_9229insTTCTTTCAGT NP_000072.2:p.Lys3077PhefsTer4
NM_001301365.1:c.9228_9229insTTCTTTCAGT , LRG_143t2:c.9228_9229insTTCTTTCAGT NP_001288294.1:p.Lys3077PhefsTer4
XM_011544031.1:c.9390_9391insTTCTTTCAGT XP_011542333.1:p.Lys3131PhefsTer4
XM_011544032.1:c.9390_9391insTTCTTTCAGT XP_011542334.1:p.Lys3131PhefsTer4
XM_011544033.1:c.9390_9391insTTCTTTCAGT XP_011542335.1:p.Lys3131PhefsTer4
XM_011544034.1:c.9252_9253insTTCTTTCAGT XP_011542336.1:p.Lys3085PhefsTer4
XM_011544035.1:c.9390_9391insTTCTTTCAGT XP_011542337.1:p.Lys3131PhefsTer4
XM_011544036.1:c.7053_7054insTTCTTTCAGT XP_011542338.1:p.Lys2352PhefsTer4
XM_011544033.2:c.9390_9391insTTCTTTCAGT XP_011542335.1:p.Lys3131PhefsTer4
XM_011544035.2:c.9390_9391insTTCTTTCAGT XP_011542337.1:p.Lys3131PhefsTer4
XM_011544036.2:c.7053_7054insTTCTTTCAGT XP_011542338.1:p.Lys2352PhefsTer4
XM_017000150.1:c.9390_9391insTTCTTTCAGT XP_016855639.1:p.Lys3131PhefsTer4
XR_001736947.1:n.10263_10264insTTCTTTCAGT
NM_000081.4:c.9228_9229insTTCTTTCAGT MANE Select NP_000072.2:p.Lys3077PhefsTer4
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