Canonical Allele Identifier: CA2551110009
Gene: RERE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8358152_8358154dup , CM000663.2:g.8358152_8358154dup GRCh38
NC_000001.10:g.8418212_8418214dup , CM000663.1:g.8418212_8418214dup GRCh37
NC_000001.9:g.8340799_8340801dup NCBI36
NG_047035.1:g.464539_464541dup

Transcript Alleles

HGVS Amino-acid change
ENST00000465125.2:c.2677+43_2677+45dup ENSP00000515651.1:n.2677+43_2677+45dup
ENST00000400908.7:c.4339+43_4339+45dup MANE Select ENSP00000383700.2:n.4339+43_4339+45dup
ENST00000337907.7:c.4339+43_4339+45dup ENSP00000338629.3:n.4339+43_4339+45dup
ENST00000377464.5:c.3535+43_3535+45dup ENSP00000366684.1:n.3535+43_3535+45dup
ENST00000400907.6:c.1541-2554_1541-2552dup ENSP00000383699.2:n.1541-2554_1541-2552dup
ENST00000400908.6:c.4339+43_4339+45dup ENSP00000383700.2:n.4339+43_4339+45dup
ENST00000476556.5:c.2677+43_2677+45dup ENSP00000422246.1:n.2677+43_2677+45dup
ENST00000505225.1:c.308-1907_308-1905dup ENSP00000423451.1:n.308-1907_308-1905dup
NM_001042681.1:c.4339+43_4339+45dup NP_001036146.1:n.4339+43_4339+45dup
NM_001042682.1:c.2677+43_2677+45dup NP_001036147.1:n.2677+43_2677+45dup
NM_012102.3:c.4339+43_4339+45dup NP_036234.3:n.4339+43_4339+45dup
XM_005263464.1:c.4339+43_4339+45dup XP_005263521.1:n.4339+43_4339+45dup
XM_005263466.1:c.3535+43_3535+45dup XP_005263523.1:n.3535+43_3535+45dup
XM_006710653.1:c.4339+43_4339+45dup XP_006710716.1:n.4339+43_4339+45dup
XM_011541510.1:c.4213+43_4213+45dup XP_011539812.1:n.4213+43_4213+45dup
XM_005263464.2:c.4339+43_4339+45dup XP_005263521.1:n.4339+43_4339+45dup
XM_011541510.2:c.4213+43_4213+45dup XP_011539812.1:n.4213+43_4213+45dup
XM_017001358.1:c.4339+43_4339+45dup XP_016856847.1:n.4339+43_4339+45dup
XM_017001359.1:c.4339+43_4339+45dup XP_016856848.1:n.4339+43_4339+45dup
NM_001042681.2:c.4339+43_4339+45dup MANE Select NP_001036146.1:n.4339+43_4339+45dup
NM_001042682.2:c.2677+43_2677+45dup NP_001036147.1:n.2677+43_2677+45dup
NM_012102.4:c.4339+43_4339+45dup NP_036234.3:n.4339+43_4339+45dup