Canonical Allele Identifier: CA1152436202

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8699326_8699330delinsTCAGA , CM000663.2:g.8699326_8699330delinsTCAGA	GRCh38
NC_000001.10:g.8759385_8759389delinsTCAGA , CM000663.1:g.8759385_8759389delinsTCAGA	GRCh37
NC_000001.9:g.8681972_8681976delinsTCAGA	NCBI36
NG_047035.1:g.123362_123366delinsTCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704050.1:c.-145+25230_-145+25234delinsTCTGA	ENSP00000515653.1:n.-145+25230_-145+25234delinsTCTGA
ENST00000400908.7:c.-144-42889_-144-42885delinsTCTGA MANE Select	ENSP00000383700.2:n.-144-42889_-144-42885delinsTCTGA
ENST00000656437.1:c.-144-42889_-144-42885delinsTCTGA	ENSP00000499322.1:n.-144-42889_-144-42885delinsTCTGA
ENST00000659924.1:c.-144-42889_-144-42885delinsTCTGA	ENSP00000499704.1:n.-144-42889_-144-42885delinsTCTGA
ENST00000337907.7:c.-144-42889_-144-42885delinsTCTGA	ENSP00000338629.3:n.-144-42889_-144-42885delinsTCTGA
ENST00000400908.6:c.-144-42889_-144-42885delinsTCTGA	ENSP00000383700.2:n.-144-42889_-144-42885delinsTCTGA
ENST00000468247.1:c.-145+3725_-145+3729delinsTCTGA	ENSP00000465271.1:n.-145+3725_-145+3729delinsTCTGA
ENST00000480342.5:n.409-42889_409-42885delinsTCTGA
NM_001042681.1:c.-144-42889_-144-42885delinsTCTGA	NP_001036146.1:n.-144-42889_-144-42885delinsTCTGA
NM_012102.3:c.-144-42889_-144-42885delinsTCTGA	NP_036234.3:n.-144-42889_-144-42885delinsTCTGA
XM_005263464.1:c.-145+3725_-145+3729delinsTCTGA	XP_005263521.1:n.-145+3725_-145+3729delinsTCTGA
XM_006710653.1:c.-144-42889_-144-42885delinsTCTGA	XP_006710716.1:n.-144-42889_-144-42885delinsTCTGA
XM_011541510.1:c.-144-42889_-144-42885delinsTCTGA	XP_011539812.1:n.-144-42889_-144-42885delinsTCTGA
XM_011541511.1:c.-144-42889_-144-42885delinsTCTGA	XP_011539813.1:n.-144-42889_-144-42885delinsTCTGA
XM_005263464.2:c.-145+3725_-145+3729delinsTCTGA	XP_005263521.1:n.-145+3725_-145+3729delinsTCTGA
XM_011541510.2:c.-144-42889_-144-42885delinsTCTGA	XP_011539812.1:n.-144-42889_-144-42885delinsTCTGA
XM_011541511.2:c.-144-42889_-144-42885delinsTCTGA	XP_011539813.1:n.-144-42889_-144-42885delinsTCTGA
XM_017001358.1:c.-144-42889_-144-42885delinsTCTGA	XP_016856847.1:n.-144-42889_-144-42885delinsTCTGA
XM_017001359.1:c.-145+37553_-145+37557delinsTCTGA	XP_016856848.1:n.-145+37553_-145+37557delinsTCTGA
NM_001042681.2:c.-144-42889_-144-42885delinsTCTGA MANE Select	NP_001036146.1:n.-144-42889_-144-42885delinsTCTGA
NM_012102.4:c.-144-42889_-144-42885delinsTCTGA	NP_036234.3:n.-144-42889_-144-42885delinsTCTGA