Canonical Allele Identifier: CA17695016
Gene: RERE HGNC NCBI

Linked Data

ClinVar Variation Id: 2435402
ClinVar RCV Id: RCV003135223
dbSNP Id: rs977359991
gnomAD v2: 1-8420431-G-A
gnomAD v3: 1-8360371-G-A
gnomAD v4: 1-8360371-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8360371G>A , CM000663.2:g.8360371G>A GRCh38
NC_000001.10:g.8420431G>A , CM000663.1:g.8420431G>A GRCh37
NC_000001.9:g.8343018G>A NCBI36
NG_047035.1:g.462321C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.1474C>T ENSP00000515651.1:p.Pro492Ser
ENST00000400908.7:c.3136C>T MANE Select ENSP00000383700.2:p.Pro1046Ser
ENST00000337907.7:c.3136C>T ENSP00000338629.3:p.Pro1046Ser
ENST00000377464.5:c.2332C>T ENSP00000366684.1:p.Pro778Ser
ENST00000400907.6:c.1540+4375C>T ENSP00000383699.2:n.1540+4375C>T
ENST00000400908.6:c.3136C>T ENSP00000383700.2:p.Pro1046Ser
ENST00000476556.5:c.1474C>T ENSP00000422246.1:p.Pro492Ser
ENST00000505225.1:c.307+1089C>T ENSP00000423451.1:n.307+1089C>T
NM_001042681.1:c.3136C>T NP_001036146.1:p.Pro1046Ser
NM_001042682.1:c.1474C>T NP_001036147.1:p.Pro492Ser
NM_012102.3:c.3136C>T NP_036234.3:p.Pro1046Ser
XM_005263464.1:c.3136C>T XP_005263521.1:p.Pro1046Ser
XM_005263466.1:c.2332C>T XP_005263523.1:p.Pro778Ser
XM_006710653.1:c.3136C>T XP_006710716.1:p.Pro1046Ser
XM_011541510.1:c.3010C>T XP_011539812.1:p.Pro1004Ser
XM_011541511.1:c.3136C>T XP_011539813.1:p.Pro1046Ser
XM_005263464.2:c.3136C>T XP_005263521.1:p.Pro1046Ser
XM_011541510.2:c.3010C>T XP_011539812.1:p.Pro1004Ser
XM_011541511.2:c.3136C>T XP_011539813.1:p.Pro1046Ser
XM_017001358.1:c.3136C>T XP_016856847.1:p.Pro1046Ser
XM_017001359.1:c.3136C>T XP_016856848.1:p.Pro1046Ser
NM_001042681.2:c.3136C>T MANE Select NP_001036146.1:p.Pro1046Ser
NM_001042682.2:c.1474C>T NP_001036147.1:p.Pro492Ser
NM_012102.4:c.3136C>T NP_036234.3:p.Pro1046Ser