Canonical Allele Identifier: CA2643066454
Gene: RERE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8360044_8360045insAA , CM000663.2:g.8360044_8360045insAA GRCh38
NC_000001.10:g.8420104_8420105insAA , CM000663.1:g.8420104_8420105insAA GRCh37
NC_000001.9:g.8342691_8342692insAA NCBI36
NG_047035.1:g.462647_462648insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.1734-59_1734-58insTT ENSP00000515651.1:n.1734-59_1734-58insTT
ENST00000400908.7:c.3396-59_3396-58insTT MANE Select ENSP00000383700.2:n.3396-59_3396-58insTT
ENST00000337907.7:c.3396-59_3396-58insTT ENSP00000338629.3:n.3396-59_3396-58insTT
ENST00000377464.5:c.2592-59_2592-58insTT ENSP00000366684.1:n.2592-59_2592-58insTT
ENST00000400907.6:c.1541-4446_1541-4445insTT ENSP00000383699.2:n.1541-4446_1541-4445insTT
ENST00000400908.6:c.3396-59_3396-58insTT ENSP00000383700.2:n.3396-59_3396-58insTT
ENST00000476556.5:c.1734-59_1734-58insTT ENSP00000422246.1:n.1734-59_1734-58insTT
ENST00000505225.1:c.307+1415_307+1416insTT ENSP00000423451.1:n.307+1415_307+1416insTT
NM_001042681.1:c.3396-59_3396-58insTT NP_001036146.1:n.3396-59_3396-58insTT
NM_001042682.1:c.1734-59_1734-58insTT NP_001036147.1:n.1734-59_1734-58insTT
NM_012102.3:c.3396-59_3396-58insTT NP_036234.3:n.3396-59_3396-58insTT
XM_005263464.1:c.3396-59_3396-58insTT XP_005263521.1:n.3396-59_3396-58insTT
XM_005263466.1:c.2592-59_2592-58insTT XP_005263523.1:n.2592-59_2592-58insTT
XM_006710653.1:c.3396-59_3396-58insTT XP_006710716.1:n.3396-59_3396-58insTT
XM_011541510.1:c.3270-59_3270-58insTT XP_011539812.1:n.3270-59_3270-58insTT
XM_011541511.1:c.3395+67_3395+68insTT XP_011539813.1:n.3395+67_3395+68insTT
XM_005263464.2:c.3396-59_3396-58insTT XP_005263521.1:n.3396-59_3396-58insTT
XM_011541510.2:c.3270-59_3270-58insTT XP_011539812.1:n.3270-59_3270-58insTT
XM_011541511.2:c.3395+67_3395+68insTT XP_011539813.1:n.3395+67_3395+68insTT
XM_017001358.1:c.3396-59_3396-58insTT XP_016856847.1:n.3396-59_3396-58insTT
XM_017001359.1:c.3396-59_3396-58insTT XP_016856848.1:n.3396-59_3396-58insTT
NM_001042681.2:c.3396-59_3396-58insTT MANE Select NP_001036146.1:n.3396-59_3396-58insTT
NM_001042682.2:c.1734-59_1734-58insTT NP_001036147.1:n.1734-59_1734-58insTT
NM_012102.4:c.3396-59_3396-58insTT NP_036234.3:n.3396-59_3396-58insTT