Canonical Allele Identifier: CA1930186764

Gene: LCOR

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.96880162_96880164delinsTGA , CM000672.2:g.96880162_96880164delinsTGA	GRCh38
NC_000010.10:g.98639919_98639921delinsTGA , CM000672.1:g.98639919_98639921delinsTGA	GRCh37
NC_000010.9:g.98629909_98629911delinsTGA	NCBI36
NG_051561.2:g.52903_52905delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371103.8:c.-329-27103_-329-27101delinsTGA	ENSP00000360144.3:n.-329-27103_-329-27101delinsTGA
ENST00000421806.4:c.-329-27103_-329-27101delinsTGA MANE Select	ENSP00000490116.2:n.-329-27103_-329-27101delinsTGA
ENST00000540664.6:c.-329-27103_-329-27101delinsTGA	ENSP00000443431.1:n.-329-27103_-329-27101delinsTGA
ENST00000674725.1:c.152-27103_152-27101delinsTGA	ENSP00000502416.1:n.152-27103_152-27101delinsTGA
ENST00000674796.1:c.74-27103_74-27101delinsTGA	ENSP00000502397.1:n.74-27103_74-27101delinsTGA
ENST00000675117.1:c.74-27103_74-27101delinsTGA	ENSP00000502330.1:n.74-27103_74-27101delinsTGA
ENST00000675125.1:c.82-27103_82-27101delinsTGA	ENSP00000502111.1:n.82-27103_82-27101delinsTGA
ENST00000675151.1:c.*36-27103_*36-27101delinsTGA	ENSP00000502263.1:n.*36-27103_*36-27101delinsTGA
ENST00000675251.1:c.47-4241_47-4239delinsTGA	ENSP00000501787.1:n.47-4241_47-4239delinsTGA
ENST00000675471.1:c.-340-27103_-340-27101delinsTGA	ENSP00000502633.1:n.-340-27103_-340-27101delinsTGA
ENST00000675537.1:c.-329-27103_-329-27101delinsTGA	ENSP00000501560.1:n.-329-27103_-329-27101delinsTGA
ENST00000675687.1:c.-329-27103_-329-27101delinsTGA	ENSP00000502138.1:n.-329-27103_-329-27101delinsTGA
ENST00000675902.1:c.156-27103_156-27101delinsTGA	ENSP00000502127.1:n.156-27103_156-27101delinsTGA
ENST00000675915.1:c.264+21746_264+21748delinsTGA
ENST00000675971.1:c.-329-27103_-329-27101delinsTGA	ENSP00000501639.1:n.-329-27103_-329-27101delinsTGA
ENST00000676067.1:c.*36-27103_*36-27101delinsTGA	ENSP00000502465.1:n.*36-27103_*36-27101delinsTGA
ENST00000676123.1:c.98-27103_98-27101delinsTGA	ENSP00000501887.1:n.98-27103_98-27101delinsTGA
ENST00000676187.1:c.47-27103_47-27101delinsTGA	ENSP00000502316.1:n.47-27103_47-27101delinsTGA
ENST00000676257.1:c.94-27103_94-27101delinsTGA	ENSP00000501998.1:n.94-27103_94-27101delinsTGA
ENST00000676314.1:c.199+21746_199+21748delinsTGA
ENST00000676373.1:n.152-27103_152-27101delinsTGA
ENST00000676381.1:c.233-27103_233-27101delinsTGA	ENSP00000501937.1:n.233-27103_233-27101delinsTGA
ENST00000676414.1:c.-329-27103_-329-27101delinsTGA	ENSP00000502500.1:n.-329-27103_-329-27101delinsTGA
ENST00000356016.7:c.-329-27103_-329-27101delinsTGA	ENSP00000348298.2:n.-329-27103_-329-27101delinsTGA
ENST00000371097.8:c.-329-27103_-329-27101delinsTGA	ENSP00000360138.3:n.-329-27103_-329-27101delinsTGA
ENST00000371103.7:c.-329-27103_-329-27101delinsTGA	ENSP00000360144.3:n.-329-27103_-329-27101delinsTGA
ENST00000540664.5:c.-329-27103_-329-27101delinsTGA	ENSP00000443431.1:n.-329-27103_-329-27101delinsTGA
NM_001170765.1:c.-329-27103_-329-27101delinsTGA	NP_001164236.1:n.-329-27103_-329-27101delinsTGA
NM_001170766.1:c.-329-27103_-329-27101delinsTGA	NP_001164237.1:n.-329-27103_-329-27101delinsTGA
NM_032440.3:c.-329-27103_-329-27101delinsTGA	NP_115816.2:n.-329-27103_-329-27101delinsTGA
XM_006718033.2:c.152-27103_152-27101delinsTGA	XP_006718096.1:n.152-27103_152-27101delinsTGA
XM_006718034.2:c.-329-27103_-329-27101delinsTGA	XP_006718097.1:n.-329-27103_-329-27101delinsTGA
XM_011540277.1:c.152-27103_152-27101delinsTGA	XP_011538579.1:n.152-27103_152-27101delinsTGA
NM_001346516.1:c.-329-27103_-329-27101delinsTGA	NP_001333445.1:n.-329-27103_-329-27101delinsTGA
NM_001170765.2:c.-329-27103_-329-27101delinsTGA	NP_001164236.1:n.-329-27103_-329-27101delinsTGA
NM_001170766.2:c.-329-27103_-329-27101delinsTGA	NP_001164237.1:n.-329-27103_-329-27101delinsTGA
NM_001346516.2:c.-329-27103_-329-27101delinsTGA MANE Select	NP_001333445.1:n.-329-27103_-329-27101delinsTGA
NM_032440.4:c.-329-27103_-329-27101delinsTGA	NP_115816.2:n.-329-27103_-329-27101delinsTGA