Canonical Allele Identifier: CA953797579
Gene: CRYL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20476360_20476371dup , CM000675.2:g.20476360_20476371dup GRCh38
NC_000013.10:g.21050499_21050510dup , CM000675.1:g.21050499_21050510dup GRCh37
NC_000013.9:g.19948499_19948510dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000298248.12:c.276+13004_276+13015dup MANE Select ENSP00000298248.7:n.276+13004_276+13015dup
ENST00000643035.1:c.*77+505_*77+516dup ENSP00000496154.1:n.*77+505_*77+516dup
ENST00000643750.1:c.210+13004_210+13015dup ENSP00000493818.1:n.210+13004_210+13015dup
ENST00000643887.1:c.276+13004_276+13015dup ENSP00000495342.1:n.276+13004_276+13015dup
ENST00000644153.1:c.277-3292_277-3281dup ENSP00000494794.1:n.277-3292_277-3281dup
ENST00000644167.1:c.276+13004_276+13015dup ENSP00000494114.1:n.276+13004_276+13015dup
ENST00000644593.1:c.276+13004_276+13015dup ENSP00000493784.1:n.276+13004_276+13015dup
ENST00000644872.1:n.233+13004_233+13015dup
ENST00000298248.11:c.276+13004_276+13015dup ENSP00000298248.7:n.276+13004_276+13015dup
ENST00000382812.5:c.210+13004_210+13015dup ENSP00000372262.1:n.210+13004_210+13015dup
ENST00000480748.2:c.67+13004_67+13015dup
NM_015974.2:c.276+13004_276+13015dup NP_057058.2:n.276+13004_276+13015dup
XM_005266415.2:c.276+13004_276+13015dup XP_005266472.1:n.276+13004_276+13015dup
XM_005266416.3:c.276+13004_276+13015dup XP_005266473.1:n.276+13004_276+13015dup
XM_011535100.1:c.276+13004_276+13015dup XP_011533402.1:n.276+13004_276+13015dup
XM_011535101.1:c.276+13004_276+13015dup XP_011533403.1:n.276+13004_276+13015dup
NM_001363647.1:c.276+13004_276+13015dup NP_001350576.1:n.276+13004_276+13015dup
XM_005266416.5:c.276+13004_276+13015dup XP_005266473.1:n.276+13004_276+13015dup
XM_017020624.1:c.-88-3292_-88-3281dup XP_016876113.1:n.-88-3292_-88-3281dup
NM_015974.3:c.276+13004_276+13015dup MANE Select NP_057058.2:n.276+13004_276+13015dup
NM_001363647.2:c.276+13004_276+13015dup NP_001350576.1:n.276+13004_276+13015dup