Canonical Allele Identifier: CA1930186759

Gene: LCOR

Linked Data

• dbSNP Id: rs1589627416

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.96880154G>T , CM000672.2:g.96880154G>T	GRCh38
NC_000010.10:g.98639911G>T , CM000672.1:g.98639911G>T	GRCh37
NC_000010.9:g.98629901G>T	NCBI36
NG_051561.2:g.52895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371103.8:c.-329-27111G>T	ENSP00000360144.3:n.-329-27111G>T
ENST00000421806.4:c.-329-27111G>T MANE Select	ENSP00000490116.2:n.-329-27111G>T
ENST00000540664.6:c.-329-27111G>T	ENSP00000443431.1:n.-329-27111G>T
ENST00000674725.1:c.152-27111G>T	ENSP00000502416.1:n.152-27111G>T
ENST00000674796.1:c.74-27111G>T	ENSP00000502397.1:n.74-27111G>T
ENST00000675117.1:c.74-27111G>T	ENSP00000502330.1:n.74-27111G>T
ENST00000675125.1:c.82-27111G>T	ENSP00000502111.1:n.82-27111G>T
ENST00000675151.1:c.*36-27111G>T	ENSP00000502263.1:n.*36-27111G>T
ENST00000675251.1:c.47-4249G>T	ENSP00000501787.1:n.47-4249G>T
ENST00000675471.1:c.-340-27111G>T	ENSP00000502633.1:n.-340-27111G>T
ENST00000675537.1:c.-329-27111G>T	ENSP00000501560.1:n.-329-27111G>T
ENST00000675687.1:c.-329-27111G>T	ENSP00000502138.1:n.-329-27111G>T
ENST00000675902.1:c.156-27111G>T	ENSP00000502127.1:n.156-27111G>T
ENST00000675915.1:c.264+21738G>T
ENST00000675971.1:c.-329-27111G>T	ENSP00000501639.1:n.-329-27111G>T
ENST00000676067.1:c.*36-27111G>T	ENSP00000502465.1:n.*36-27111G>T
ENST00000676123.1:c.98-27111G>T	ENSP00000501887.1:n.98-27111G>T
ENST00000676187.1:c.47-27111G>T	ENSP00000502316.1:n.47-27111G>T
ENST00000676257.1:c.94-27111G>T	ENSP00000501998.1:n.94-27111G>T
ENST00000676314.1:c.199+21738G>T
ENST00000676373.1:n.152-27111G>T
ENST00000676381.1:c.233-27111G>T	ENSP00000501937.1:n.233-27111G>T
ENST00000676414.1:c.-329-27111G>T	ENSP00000502500.1:n.-329-27111G>T
ENST00000356016.7:c.-329-27111G>T	ENSP00000348298.2:n.-329-27111G>T
ENST00000371097.8:c.-329-27111G>T	ENSP00000360138.3:n.-329-27111G>T
ENST00000371103.7:c.-329-27111G>T	ENSP00000360144.3:n.-329-27111G>T
ENST00000540664.5:c.-329-27111G>T	ENSP00000443431.1:n.-329-27111G>T
NM_001170765.1:c.-329-27111G>T	NP_001164236.1:n.-329-27111G>T
NM_001170766.1:c.-329-27111G>T	NP_001164237.1:n.-329-27111G>T
NM_032440.3:c.-329-27111G>T	NP_115816.2:n.-329-27111G>T
XM_006718033.2:c.152-27111G>T	XP_006718096.1:n.152-27111G>T
XM_006718034.2:c.-329-27111G>T	XP_006718097.1:n.-329-27111G>T
XM_011540277.1:c.152-27111G>T	XP_011538579.1:n.152-27111G>T
NM_001346516.1:c.-329-27111G>T	NP_001333445.1:n.-329-27111G>T
NM_001170765.2:c.-329-27111G>T	NP_001164236.1:n.-329-27111G>T
NM_001170766.2:c.-329-27111G>T	NP_001164237.1:n.-329-27111G>T
NM_001346516.2:c.-329-27111G>T MANE Select	NP_001333445.1:n.-329-27111G>T
NM_032440.4:c.-329-27111G>T	NP_115816.2:n.-329-27111G>T