Canonical Allele Identifier: CA2077292213
Gene: CRYL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20476353_20476354delinsTC , CM000675.2:g.20476353_20476354delinsTC GRCh38
NC_000013.10:g.21050492_21050493delinsTC , CM000675.1:g.21050492_21050493delinsTC GRCh37
NC_000013.9:g.19948492_19948493delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000298248.12:c.276+13016_276+13017delinsGA MANE Select ENSP00000298248.7:n.276+13016_276+13017delinsGA
ENST00000643035.1:c.*77+517_*77+518delinsGA ENSP00000496154.1:n.*77+517_*77+518delinsGA
ENST00000643750.1:c.210+13016_210+13017delinsGA ENSP00000493818.1:n.210+13016_210+13017delinsGA
ENST00000643887.1:c.276+13016_276+13017delinsGA ENSP00000495342.1:n.276+13016_276+13017delinsGA
ENST00000644153.1:c.277-3280_277-3279delinsGA ENSP00000494794.1:n.277-3280_277-3279delinsGA
ENST00000644167.1:c.276+13016_276+13017delinsGA ENSP00000494114.1:n.276+13016_276+13017delinsGA
ENST00000644593.1:c.276+13016_276+13017delinsGA ENSP00000493784.1:n.276+13016_276+13017delinsGA
ENST00000644872.1:n.233+13016_233+13017delinsGA
ENST00000298248.11:c.276+13016_276+13017delinsGA ENSP00000298248.7:n.276+13016_276+13017delinsGA
ENST00000382812.5:c.210+13016_210+13017delinsGA ENSP00000372262.1:n.210+13016_210+13017delinsGA
ENST00000480748.2:c.67+13016_67+13017delinsGA
NM_015974.2:c.276+13016_276+13017delinsGA NP_057058.2:n.276+13016_276+13017delinsGA
XM_005266415.2:c.276+13016_276+13017delinsGA XP_005266472.1:n.276+13016_276+13017delinsGA
XM_005266416.3:c.276+13016_276+13017delinsGA XP_005266473.1:n.276+13016_276+13017delinsGA
XM_011535100.1:c.276+13016_276+13017delinsGA XP_011533402.1:n.276+13016_276+13017delinsGA
XM_011535101.1:c.276+13016_276+13017delinsGA XP_011533403.1:n.276+13016_276+13017delinsGA
NM_001363647.1:c.276+13016_276+13017delinsGA NP_001350576.1:n.276+13016_276+13017delinsGA
XM_005266416.5:c.276+13016_276+13017delinsGA XP_005266473.1:n.276+13016_276+13017delinsGA
XM_017020624.1:c.-88-3280_-88-3279delinsGA XP_016876113.1:n.-88-3280_-88-3279delinsGA
NM_015974.3:c.276+13016_276+13017delinsGA MANE Select NP_057058.2:n.276+13016_276+13017delinsGA
NM_001363647.2:c.276+13016_276+13017delinsGA NP_001350576.1:n.276+13016_276+13017delinsGA