Canonical Allele Identifier: CA338168091
Gene: RERE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8355470C>G , CM000663.2:g.8355470C>G GRCh38
NC_000001.10:g.8415530C>G , CM000663.1:g.8415530C>G GRCh37
NC_000001.9:g.8338117C>G NCBI36
NG_047035.1:g.467222G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.2954G>C ENSP00000515651.1:p.Gly985Ala
ENST00000400908.7:c.4616G>C MANE Select ENSP00000383700.2:p.Gly1539Ala
ENST00000337907.7:c.4616G>C ENSP00000338629.3:p.Gly1539Ala
ENST00000377464.5:c.3812G>C ENSP00000366684.1:p.Gly1271Ala
ENST00000400907.6:c.1670G>C ENSP00000383699.2:p.Gly557Ala
ENST00000400908.6:c.4616G>C ENSP00000383700.2:p.Gly1539Ala
ENST00000476556.5:c.2954G>C ENSP00000422246.1:p.Gly985Ala
NM_001042681.1:c.4616G>C NP_001036146.1:p.Gly1539Ala
NM_001042682.1:c.2954G>C NP_001036147.1:p.Gly985Ala
NM_012102.3:c.4616G>C NP_036234.3:p.Gly1539Ala
XM_005263464.1:c.4616G>C XP_005263521.1:p.Gly1539Ala
XM_005263466.1:c.3812G>C XP_005263523.1:p.Gly1271Ala
XM_006710653.1:c.4616G>C XP_006710716.1:p.Gly1539Ala
XM_011541510.1:c.4490G>C XP_011539812.1:p.Gly1497Ala
XM_005263464.2:c.4616G>C XP_005263521.1:p.Gly1539Ala
XM_011541510.2:c.4490G>C XP_011539812.1:p.Gly1497Ala
XM_017001358.1:c.4616G>C XP_016856847.1:p.Gly1539Ala
XM_017001359.1:c.4616G>C XP_016856848.1:p.Gly1539Ala
NM_001042681.2:c.4616G>C MANE Select NP_001036146.1:p.Gly1539Ala
NM_001042682.2:c.2954G>C NP_001036147.1:p.Gly985Ala
NM_012102.4:c.4616G>C NP_036234.3:p.Gly1539Ala