Canonical Allele Identifier: CA1152321095
Gene: RERE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8359912G= , CM000663.2:g.8359912G= GRCh38
NC_000001.10:g.8419972G= , CM000663.1:g.8419972G= GRCh37
NC_000001.9:g.8342559G= NCBI36
NG_047035.1:g.462780C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.1808C= ENSP00000515651.1:p.Ser603=
ENST00000400908.7:c.3470C= MANE Select ENSP00000383700.2:p.Ser1157=
ENST00000337907.7:c.3470C= ENSP00000338629.3:p.Ser1157=
ENST00000377464.5:c.2666C= ENSP00000366684.1:p.Ser889=
ENST00000400907.6:c.1541-4313C= ENSP00000383699.2:n.1541-4313C=
ENST00000400908.6:c.3470C= ENSP00000383700.2:p.Ser1157=
ENST00000476556.5:c.1808C= ENSP00000422246.1:p.Ser603=
ENST00000505225.1:c.307+1548C= ENSP00000423451.1:n.307+1548C=
NM_001042681.1:c.3470C= NP_001036146.1:p.Ser1157=
NM_001042682.1:c.1808C= NP_001036147.1:p.Ser603=
NM_012102.3:c.3470C= NP_036234.3:p.Ser1157=
XM_005263464.1:c.3470C= XP_005263521.1:p.Ser1157=
XM_005263466.1:c.2666C= XP_005263523.1:p.Ser889=
XM_006710653.1:c.3470C= XP_006710716.1:p.Ser1157=
XM_011541510.1:c.3344C= XP_011539812.1:p.Ser1115=
XM_011541511.1:c.3395+200C= XP_011539813.1:n.3395+200C=
XM_005263464.2:c.3470C= XP_005263521.1:p.Ser1157=
XM_011541510.2:c.3344C= XP_011539812.1:p.Ser1115=
XM_011541511.2:c.3395+200C= XP_011539813.1:n.3395+200C=
XM_017001358.1:c.3470C= XP_016856847.1:p.Ser1157=
XM_017001359.1:c.3470C= XP_016856848.1:p.Ser1157=
NM_001042681.2:c.3470C= MANE Select NP_001036146.1:p.Ser1157=
NM_001042682.2:c.1808C= NP_001036147.1:p.Ser603=
NM_012102.4:c.3470C= NP_036234.3:p.Ser1157=