Canonical Allele Identifier: CA2740107303

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8699501A>G , CM000663.2:g.8699501A>G	GRCh38
NC_000001.10:g.8759560A>G , CM000663.1:g.8759560A>G	GRCh37
NC_000001.9:g.8682147A>G	NCBI36
NG_047035.1:g.123191T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000704050.1:c.-145+25059T>C	ENSP00000515653.1:n.-145+25059T>C
ENST00000400908.7:c.-144-43060T>C MANE Select	ENSP00000383700.2:n.-144-43060T>C
ENST00000656437.1:c.-144-43060T>C	ENSP00000499322.1:n.-144-43060T>C
ENST00000659924.1:c.-144-43060T>C	ENSP00000499704.1:n.-144-43060T>C
ENST00000337907.7:c.-144-43060T>C	ENSP00000338629.3:n.-144-43060T>C
ENST00000400908.6:c.-144-43060T>C	ENSP00000383700.2:n.-144-43060T>C
ENST00000468247.1:c.-145+3554T>C	ENSP00000465271.1:n.-145+3554T>C
ENST00000480342.5:n.409-43060T>C
NM_001042681.1:c.-144-43060T>C	NP_001036146.1:n.-144-43060T>C
NM_012102.3:c.-144-43060T>C	NP_036234.3:n.-144-43060T>C
XM_005263464.1:c.-145+3554T>C	XP_005263521.1:n.-145+3554T>C
XM_006710653.1:c.-144-43060T>C	XP_006710716.1:n.-144-43060T>C
XM_011541510.1:c.-144-43060T>C	XP_011539812.1:n.-144-43060T>C
XM_011541511.1:c.-144-43060T>C	XP_011539813.1:n.-144-43060T>C
XM_005263464.2:c.-145+3554T>C	XP_005263521.1:n.-145+3554T>C
XM_011541510.2:c.-144-43060T>C	XP_011539812.1:n.-144-43060T>C
XM_011541511.2:c.-144-43060T>C	XP_011539813.1:n.-144-43060T>C
XM_017001358.1:c.-144-43060T>C	XP_016856847.1:n.-144-43060T>C
XM_017001359.1:c.-145+37382T>C	XP_016856848.1:n.-145+37382T>C
NM_001042681.2:c.-144-43060T>C MANE Select	NP_001036146.1:n.-144-43060T>C
NM_012102.4:c.-144-43060T>C	NP_036234.3:n.-144-43060T>C