Canonical Allele Identifier: CA343835
Gene: LYST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235728077_235728132del , CM000663.2:g.235728077_235728132del GRCh38
NC_000001.10:g.235891377_235891432del , CM000663.1:g.235891377_235891432del GRCh37
NC_000001.9:g.233958000_233958055del NCBI36
NG_007397.1:g.160512_160567del , LRG_143:g.160512_160567del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461526.2:c.4637_4690+2del
ENST00000475277.2:c.1204_1257+2del
ENST00000697178.1:c.*4533_*4586+2del
ENST00000697236.1:c.2818_2871+2del
ENST00000697237.1:c.65_118+2del
ENST00000697240.1:c.1243_1296+2del
ENST00000697241.1:c.3589_3642+2del
ENST00000389793.7:c.9109_9162+2del
ENST00000389793.6:c.9109_9162+2del
ENST00000389794.7:c.*4533_*4586+2del
ENST00000473037.5:n.4099_4152+2del
NM_000081.3:c.9109_9162+2del , LRG_143t1:c.9109_9162+2del
NM_001301365.1:c.9109_9162+2del , LRG_143t2:c.9109_9162+2del
XM_011544031.1:c.9271_9324+2del
XM_011544032.1:c.9271_9324+2del
XM_011544033.1:c.9271_9324+2del
XM_011544034.1:c.9133_9186+2del
XM_011544035.1:c.9271_9324+2del
XM_011544036.1:c.6934_6987+2del
XM_011544033.2:c.9271_9324+2del
XM_011544035.2:c.9271_9324+2del
XM_011544036.2:c.6934_6987+2del
XM_017000150.1:c.9271_9324+2del
XR_001736947.1:n.10144_10197+2del
NM_000081.4:c.9109_9162+2del