Canonical Allele Identifier: CA1152436248

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8699450_8699451delinsAT , CM000663.2:g.8699450_8699451delinsAT	GRCh38
NC_000001.10:g.8759509_8759510delinsAT , CM000663.1:g.8759509_8759510delinsAT	GRCh37
NC_000001.9:g.8682096_8682097delinsAT	NCBI36
NG_047035.1:g.123241_123242delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704050.1:c.-145+25109_-145+25110delinsAT	ENSP00000515653.1:n.-145+25109_-145+25110delinsAT
ENST00000400908.7:c.-144-43010_-144-43009delinsAT MANE Select	ENSP00000383700.2:n.-144-43010_-144-43009delinsAT
ENST00000656437.1:c.-144-43010_-144-43009delinsAT	ENSP00000499322.1:n.-144-43010_-144-43009delinsAT
ENST00000659924.1:c.-144-43010_-144-43009delinsAT	ENSP00000499704.1:n.-144-43010_-144-43009delinsAT
ENST00000337907.7:c.-144-43010_-144-43009delinsAT	ENSP00000338629.3:n.-144-43010_-144-43009delinsAT
ENST00000400908.6:c.-144-43010_-144-43009delinsAT	ENSP00000383700.2:n.-144-43010_-144-43009delinsAT
ENST00000468247.1:c.-145+3604_-145+3605delinsAT	ENSP00000465271.1:n.-145+3604_-145+3605delinsAT
ENST00000480342.5:n.409-43010_409-43009delinsAT
NM_001042681.1:c.-144-43010_-144-43009delinsAT	NP_001036146.1:n.-144-43010_-144-43009delinsAT
NM_012102.3:c.-144-43010_-144-43009delinsAT	NP_036234.3:n.-144-43010_-144-43009delinsAT
XM_005263464.1:c.-145+3604_-145+3605delinsAT	XP_005263521.1:n.-145+3604_-145+3605delinsAT
XM_006710653.1:c.-144-43010_-144-43009delinsAT	XP_006710716.1:n.-144-43010_-144-43009delinsAT
XM_011541510.1:c.-144-43010_-144-43009delinsAT	XP_011539812.1:n.-144-43010_-144-43009delinsAT
XM_011541511.1:c.-144-43010_-144-43009delinsAT	XP_011539813.1:n.-144-43010_-144-43009delinsAT
XM_005263464.2:c.-145+3604_-145+3605delinsAT	XP_005263521.1:n.-145+3604_-145+3605delinsAT
XM_011541510.2:c.-144-43010_-144-43009delinsAT	XP_011539812.1:n.-144-43010_-144-43009delinsAT
XM_011541511.2:c.-144-43010_-144-43009delinsAT	XP_011539813.1:n.-144-43010_-144-43009delinsAT
XM_017001358.1:c.-144-43010_-144-43009delinsAT	XP_016856847.1:n.-144-43010_-144-43009delinsAT
XM_017001359.1:c.-145+37432_-145+37433delinsAT	XP_016856848.1:n.-145+37432_-145+37433delinsAT
NM_001042681.2:c.-144-43010_-144-43009delinsAT MANE Select	NP_001036146.1:n.-144-43010_-144-43009delinsAT
NM_012102.4:c.-144-43010_-144-43009delinsAT	NP_036234.3:n.-144-43010_-144-43009delinsAT