Canonical Allele Identifier: CA1152318855
Gene: RERE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8355488T= , CM000663.2:g.8355488T= GRCh38
NC_000001.10:g.8415548T= , CM000663.1:g.8415548T= GRCh37
NC_000001.9:g.8338135T= NCBI36
NG_047035.1:g.467204A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.2936A= ENSP00000515651.1:p.Glu979=
ENST00000400908.7:c.4598A= MANE Select ENSP00000383700.2:p.Glu1533=
ENST00000337907.7:c.4598A= ENSP00000338629.3:p.Glu1533=
ENST00000377464.5:c.3794A= ENSP00000366684.1:p.Glu1265=
ENST00000400907.6:c.1652A= ENSP00000383699.2:p.Glu551=
ENST00000400908.6:c.4598A= ENSP00000383700.2:p.Glu1533=
ENST00000476556.5:c.2936A= ENSP00000422246.1:p.Glu979=
NM_001042681.1:c.4598A= NP_001036146.1:p.Glu1533=
NM_001042682.1:c.2936A= NP_001036147.1:p.Glu979=
NM_012102.3:c.4598A= NP_036234.3:p.Glu1533=
XM_005263464.1:c.4598A= XP_005263521.1:p.Glu1533=
XM_005263466.1:c.3794A= XP_005263523.1:p.Glu1265=
XM_006710653.1:c.4598A= XP_006710716.1:p.Glu1533=
XM_011541510.1:c.4472A= XP_011539812.1:p.Glu1491=
XM_005263464.2:c.4598A= XP_005263521.1:p.Glu1533=
XM_011541510.2:c.4472A= XP_011539812.1:p.Glu1491=
XM_017001358.1:c.4598A= XP_016856847.1:p.Glu1533=
XM_017001359.1:c.4598A= XP_016856848.1:p.Glu1533=
NM_001042681.2:c.4598A= MANE Select NP_001036146.1:p.Glu1533=
NM_001042682.2:c.2936A= NP_001036147.1:p.Glu979=
NM_012102.4:c.4598A= NP_036234.3:p.Glu1533=