Canonical Allele Identifier: CA1152436206
Gene: RERE HGNC NCBI

Linked Data

dbSNP Id: rs1639398948

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8699331C>T , CM000663.2:g.8699331C>T GRCh38
NC_000001.10:g.8759390C>T , CM000663.1:g.8759390C>T GRCh37
NC_000001.9:g.8681977C>T NCBI36
NG_047035.1:g.123361G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000704050.1:c.-145+25229G>A ENSP00000515653.1:n.-145+25229G>A
ENST00000400908.7:c.-144-42890G>A MANE Select ENSP00000383700.2:n.-144-42890G>A
ENST00000656437.1:c.-144-42890G>A ENSP00000499322.1:n.-144-42890G>A
ENST00000659924.1:c.-144-42890G>A ENSP00000499704.1:n.-144-42890G>A
ENST00000337907.7:c.-144-42890G>A ENSP00000338629.3:n.-144-42890G>A
ENST00000400908.6:c.-144-42890G>A ENSP00000383700.2:n.-144-42890G>A
ENST00000468247.1:c.-145+3724G>A ENSP00000465271.1:n.-145+3724G>A
ENST00000480342.5:n.409-42890G>A
NM_001042681.1:c.-144-42890G>A NP_001036146.1:n.-144-42890G>A
NM_012102.3:c.-144-42890G>A NP_036234.3:n.-144-42890G>A
XM_005263464.1:c.-145+3724G>A XP_005263521.1:n.-145+3724G>A
XM_006710653.1:c.-144-42890G>A XP_006710716.1:n.-144-42890G>A
XM_011541510.1:c.-144-42890G>A XP_011539812.1:n.-144-42890G>A
XM_011541511.1:c.-144-42890G>A XP_011539813.1:n.-144-42890G>A
XM_005263464.2:c.-145+3724G>A XP_005263521.1:n.-145+3724G>A
XM_011541510.2:c.-144-42890G>A XP_011539812.1:n.-144-42890G>A
XM_011541511.2:c.-144-42890G>A XP_011539813.1:n.-144-42890G>A
XM_017001358.1:c.-144-42890G>A XP_016856847.1:n.-144-42890G>A
XM_017001359.1:c.-145+37552G>A XP_016856848.1:n.-145+37552G>A
NM_001042681.2:c.-144-42890G>A MANE Select NP_001036146.1:n.-144-42890G>A
NM_012102.4:c.-144-42890G>A NP_036234.3:n.-144-42890G>A