Canonical Allele Identifier: CA1441749048

Gene: LCORL

Linked Data

• dbSNP Id: rs1725672701

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.17866481_17866485del , CM000666.2:g.17866481_17866485del	GRCh38
NC_000004.11:g.17868104_17868108del , CM000666.1:g.17868104_17868108del	GRCh37
NC_000004.10:g.17477202_17477206del	NCBI36
NG_015822.1:g.160377_160381del
NG_015822.2:g.160377_160381del

Transcript Alleles

HGVS	Amino-acid change
ENST00000635767.2:c.5602+6904_5602+6908del MANE Select	ENSP00000490600.1:n.5602+6904_5602+6908del
ENST00000635767.1:c.5602+6904_5602+6908del	ENSP00000490600.1:n.5602+6904_5602+6908del
ENST00000637787.1:c.5409+6904_5409+6908del
ENST00000675131.1:c.*604+19584_*604+19588del	ENSP00000501990.1:n.*604+19584_*604+19588del
ENST00000675143.1:c.803+515_803+519del	ENSP00000502692.1:n.803+515_803+519del
ENST00000675605.1:c.1279+515_1279+519del
ENST00000675927.1:c.801+515_801+519del
ENST00000676180.1:c.1156+515_1156+519del	ENSP00000501732.1:n.1156+515_1156+519del
ENST00000326877.8:c.776+19584_776+19588del	ENSP00000317566.3:n.776+19584_776+19588del
ENST00000510121.5:n.224+19584_224+19588del
ENST00000510451.5:c.*363-20583_*363-20579del	ENSP00000423489.1:n.*363-20583_*363-20579del
NM_153686.7:c.776+19584_776+19588del	NP_710153.2:n.776+19584_776+19588del
XM_011513821.1:c.*1+515_*1+519del	XP_011512123.1:n.*1+515_*1+519del
XM_011513822.1:c.5602+6904_5602+6908del	XP_011512124.1:n.5602+6904_5602+6908del
XM_011513823.1:c.*1+515_*1+519del	XP_011512125.1:n.*1+515_*1+519del
XM_011513824.1:c.803+515_803+519del	XP_011512126.1:n.803+515_803+519del
XM_011513826.1:c.683-20583_683-20579del	XP_011512128.1:n.683-20583_683-20579del
NM_001365660.1:c.803+515_803+519del	NP_001352589.1:n.803+515_803+519del
NM_001365663.1:c.683-20583_683-20579del	NP_001352592.1:n.683-20583_683-20579del
NM_001365665.1:c.431-20583_431-20579del	NP_001352594.1:n.431-20583_431-20579del
NM_153686.8:c.776+19584_776+19588del	NP_710153.2:n.776+19584_776+19588del
NR_136669.1:n.727-20583_727-20579del
NR_158563.1:n.803-20583_803-20579del
NR_158564.1:n.1874-20583_1874-20579del
NR_158565.1:n.1967+19584_1967+19588del
NR_158566.1:n.796-20583_796-20579del
NR_158568.1:n.820+19584_820+19588del
XM_011513821.3:c.*1+515_*1+519del	XP_011512123.1:n.*1+515_*1+519del
XM_011513822.3:c.5602+6904_5602+6908del	XP_011512124.1:n.5602+6904_5602+6908del
XM_011513823.3:c.*1+515_*1+519del	XP_011512125.1:n.*1+515_*1+519del
XM_017007961.2:c.*1+515_*1+519del	XP_016863450.1:n.*1+515_*1+519del
XM_017007962.2:c.*1+515_*1+519del	XP_016863451.1:n.*1+515_*1+519del
XM_017007963.2:c.*1+515_*1+519del	XP_016863452.1:n.*1+515_*1+519del
XM_017007965.1:c.524+19584_524+19588del	XP_016863454.1:n.524+19584_524+19588del
NR_136669.2:n.607-20583_607-20579del
NR_136669.3:n.607-20583_607-20579del
NM_001394446.1:c.5602+6904_5602+6908del MANE Select	NP_001381375.1:n.5602+6904_5602+6908del