Canonical Allele Identifier: CA1152436285
Gene: RERE HGNC NCBI

Linked Data

dbSNP Id: rs1639402941

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8699527G>C , CM000663.2:g.8699527G>C GRCh38
NC_000001.10:g.8759586G>C , CM000663.1:g.8759586G>C GRCh37
NC_000001.9:g.8682173G>C NCBI36
NG_047035.1:g.123165C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000704050.1:c.-145+25033C>G ENSP00000515653.1:n.-145+25033C>G
ENST00000400908.7:c.-144-43086C>G MANE Select ENSP00000383700.2:n.-144-43086C>G
ENST00000656437.1:c.-144-43086C>G ENSP00000499322.1:n.-144-43086C>G
ENST00000659924.1:c.-144-43086C>G ENSP00000499704.1:n.-144-43086C>G
ENST00000337907.7:c.-144-43086C>G ENSP00000338629.3:n.-144-43086C>G
ENST00000400908.6:c.-144-43086C>G ENSP00000383700.2:n.-144-43086C>G
ENST00000468247.1:c.-145+3528C>G ENSP00000465271.1:n.-145+3528C>G
ENST00000480342.5:n.409-43086C>G
NM_001042681.1:c.-144-43086C>G NP_001036146.1:n.-144-43086C>G
NM_012102.3:c.-144-43086C>G NP_036234.3:n.-144-43086C>G
XM_005263464.1:c.-145+3528C>G XP_005263521.1:n.-145+3528C>G
XM_006710653.1:c.-144-43086C>G XP_006710716.1:n.-144-43086C>G
XM_011541510.1:c.-144-43086C>G XP_011539812.1:n.-144-43086C>G
XM_011541511.1:c.-144-43086C>G XP_011539813.1:n.-144-43086C>G
XM_005263464.2:c.-145+3528C>G XP_005263521.1:n.-145+3528C>G
XM_011541510.2:c.-144-43086C>G XP_011539812.1:n.-144-43086C>G
XM_011541511.2:c.-144-43086C>G XP_011539813.1:n.-144-43086C>G
XM_017001358.1:c.-144-43086C>G XP_016856847.1:n.-144-43086C>G
XM_017001359.1:c.-145+37356C>G XP_016856848.1:n.-145+37356C>G
NM_001042681.2:c.-144-43086C>G MANE Select NP_001036146.1:n.-144-43086C>G
NM_012102.4:c.-144-43086C>G NP_036234.3:n.-144-43086C>G