Canonical Allele Identifier: CA571122
Gene: RERE HGNC NCBI

Linked Data

dbSNP Id: rs573782488
gnomAD v2: 1-8419900-T-C
gnomAD v3: 1-8359840-T-C
gnomAD v4: 1-8359840-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8359840T>C , CM000663.2:g.8359840T>C GRCh38
NC_000001.10:g.8419900T>C , CM000663.1:g.8419900T>C GRCh37
NC_000001.9:g.8342487T>C NCBI36
NG_047035.1:g.462852A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.1880A>G ENSP00000515651.1:p.Glu627Gly
ENST00000400908.7:c.3542A>G MANE Select ENSP00000383700.2:p.Glu1181Gly
ENST00000337907.7:c.3542A>G ENSP00000338629.3:p.Glu1181Gly
ENST00000377464.5:c.2738A>G ENSP00000366684.1:p.Glu913Gly
ENST00000400907.6:c.1541-4241A>G ENSP00000383699.2:n.1541-4241A>G
ENST00000400908.6:c.3542A>G ENSP00000383700.2:p.Glu1181Gly
ENST00000476556.5:c.1880A>G ENSP00000422246.1:p.Glu627Gly
ENST00000505225.1:c.307+1620A>G ENSP00000423451.1:n.307+1620A>G
NM_001042681.1:c.3542A>G NP_001036146.1:p.Glu1181Gly
NM_001042682.1:c.1880A>G NP_001036147.1:p.Glu627Gly
NM_012102.3:c.3542A>G NP_036234.3:p.Glu1181Gly
XM_005263464.1:c.3542A>G XP_005263521.1:p.Glu1181Gly
XM_005263466.1:c.2738A>G XP_005263523.1:p.Glu913Gly
XM_006710653.1:c.3542A>G XP_006710716.1:p.Glu1181Gly
XM_011541510.1:c.3416A>G XP_011539812.1:p.Glu1139Gly
XM_011541511.1:c.3395+272A>G XP_011539813.1:n.3395+272A>G
XM_005263464.2:c.3542A>G XP_005263521.1:p.Glu1181Gly
XM_011541510.2:c.3416A>G XP_011539812.1:p.Glu1139Gly
XM_011541511.2:c.3395+272A>G XP_011539813.1:n.3395+272A>G
XM_017001358.1:c.3542A>G XP_016856847.1:p.Glu1181Gly
XM_017001359.1:c.3542A>G XP_016856848.1:p.Glu1181Gly
NM_001042681.2:c.3542A>G MANE Select NP_001036146.1:p.Glu1181Gly
NM_001042682.2:c.1880A>G NP_001036147.1:p.Glu627Gly
NM_012102.4:c.3542A>G NP_036234.3:p.Glu1181Gly