Canonical Allele Identifier: CA2077292220

Gene: CRYL1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.20476354_20476363delinsCAAAAAAAAA , CM000675.2:g.20476354_20476363delinsCAAAAAAAAA	GRCh38
NC_000013.10:g.21050493_21050502delinsCAAAAAAAAA , CM000675.1:g.21050493_21050502delinsCAAAAAAAAA	GRCh37
NC_000013.9:g.19948493_19948502delinsCAAAAAAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298248.12:c.276+13007_276+13016delinsTTTTTTTTTG MANE Select	ENSP00000298248.7:n.276+13007_276+13016delinsTTTTTTTTTG
ENST00000643035.1:c.*77+508_*77+517delinsTTTTTTTTTG	ENSP00000496154.1:n.*77+508_*77+517delinsTTTTTTTTTG
ENST00000643750.1:c.210+13007_210+13016delinsTTTTTTTTTG	ENSP00000493818.1:n.210+13007_210+13016delinsTTTTTTTTTG
ENST00000643887.1:c.276+13007_276+13016delinsTTTTTTTTTG	ENSP00000495342.1:n.276+13007_276+13016delinsTTTTTTTTTG
ENST00000644153.1:c.277-3289_277-3280delinsTTTTTTTTTG	ENSP00000494794.1:n.277-3289_277-3280delinsTTTTTTTTTG
ENST00000644167.1:c.276+13007_276+13016delinsTTTTTTTTTG	ENSP00000494114.1:n.276+13007_276+13016delinsTTTTTTTTTG
ENST00000644593.1:c.276+13007_276+13016delinsTTTTTTTTTG	ENSP00000493784.1:n.276+13007_276+13016delinsTTTTTTTTTG
ENST00000644872.1:n.233+13007_233+13016delinsTTTTTTTTTG
ENST00000298248.11:c.276+13007_276+13016delinsTTTTTTTTTG	ENSP00000298248.7:n.276+13007_276+13016delinsTTTTTTTTTG
ENST00000382812.5:c.210+13007_210+13016delinsTTTTTTTTTG	ENSP00000372262.1:n.210+13007_210+13016delinsTTTTTTTTTG
ENST00000480748.2:c.67+13007_67+13016delinsTTTTTTTTTG
NM_015974.2:c.276+13007_276+13016delinsTTTTTTTTTG	NP_057058.2:n.276+13007_276+13016delinsTTTTTTTTTG
XM_005266415.2:c.276+13007_276+13016delinsTTTTTTTTTG	XP_005266472.1:n.276+13007_276+13016delinsTTTTTTTTTG
XM_005266416.3:c.276+13007_276+13016delinsTTTTTTTTTG	XP_005266473.1:n.276+13007_276+13016delinsTTTTTTTTTG
XM_011535100.1:c.276+13007_276+13016delinsTTTTTTTTTG	XP_011533402.1:n.276+13007_276+13016delinsTTTTTTTTTG
XM_011535101.1:c.276+13007_276+13016delinsTTTTTTTTTG	XP_011533403.1:n.276+13007_276+13016delinsTTTTTTTTTG
NM_001363647.1:c.276+13007_276+13016delinsTTTTTTTTTG	NP_001350576.1:n.276+13007_276+13016delinsTTTTTTTTTG
XM_005266416.5:c.276+13007_276+13016delinsTTTTTTTTTG	XP_005266473.1:n.276+13007_276+13016delinsTTTTTTTTTG
XM_017020624.1:c.-88-3289_-88-3280delinsTTTTTTTTTG	XP_016876113.1:n.-88-3289_-88-3280delinsTTTTTTTTTG
NM_015974.3:c.276+13007_276+13016delinsTTTTTTTTTG MANE Select	NP_057058.2:n.276+13007_276+13016delinsTTTTTTTTTG
NM_001363647.2:c.276+13007_276+13016delinsTTTTTTTTTG	NP_001350576.1:n.276+13007_276+13016delinsTTTTTTTTTG