Canonical Allele Identifier: CA2643066637
Gene: RERE HGNC NCBI

Linked Data

gnomAD v4: 1-8360159-CG-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8360163del , CM000663.2:g.8360163del GRCh38
NC_000001.10:g.8420223del , CM000663.1:g.8420223del GRCh37
NC_000001.9:g.8342810del NCBI36
NG_047035.1:g.462532del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.1685del ENSP00000515651.1:p.Pro562ArgfsTer?
ENST00000400908.7:c.3347del MANE Select ENSP00000383700.2:p.Pro1116ArgfsTer?
ENST00000337907.7:c.3347del ENSP00000338629.3:p.Pro1116ArgfsTer?
ENST00000377464.5:c.2543del ENSP00000366684.1:p.Pro848ArgfsTer?
ENST00000400907.6:c.1541-4561del ENSP00000383699.2:n.1541-4561del
ENST00000400908.6:c.3347del ENSP00000383700.2:p.Pro1116ArgfsTer?
ENST00000476556.5:c.1685del ENSP00000422246.1:p.Pro562ArgfsTer?
ENST00000505225.1:c.307+1300del ENSP00000423451.1:n.307+1300del
NM_001042681.1:c.3347del NP_001036146.1:p.Pro1116ArgfsTer?
NM_001042682.1:c.1685del NP_001036147.1:p.Pro562ArgfsTer?
NM_012102.3:c.3347del NP_036234.3:p.Pro1116ArgfsTer?
XM_005263464.1:c.3347del XP_005263521.1:p.Pro1116ArgfsTer?
XM_005263466.1:c.2543del XP_005263523.1:p.Pro848ArgfsTer?
XM_006710653.1:c.3347del XP_006710716.1:p.Pro1116ArgfsTer?
XM_011541510.1:c.3221del XP_011539812.1:p.Pro1074ArgfsTer?
XM_011541511.1:c.3347del XP_011539813.1:p.Pro1116ArgfsTer24
XM_005263464.2:c.3347del XP_005263521.1:p.Pro1116ArgfsTer?
XM_011541510.2:c.3221del XP_011539812.1:p.Pro1074ArgfsTer?
XM_011541511.2:c.3347del XP_011539813.1:p.Pro1116ArgfsTer24
XM_017001358.1:c.3347del XP_016856847.1:p.Pro1116ArgfsTer?
XM_017001359.1:c.3347del XP_016856848.1:p.Pro1116ArgfsTer?
NM_001042681.2:c.3347del MANE Select NP_001036146.1:p.Pro1116ArgfsTer?
NM_001042682.2:c.1685del NP_001036147.1:p.Pro562ArgfsTer?
NM_012102.4:c.3347del NP_036234.3:p.Pro1116ArgfsTer?