Canonical Allele Identifier: CA338168895
Gene: RERE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8358279A>T , CM000663.2:g.8358279A>T GRCh38
NC_000001.10:g.8418339A>T , CM000663.1:g.8418339A>T GRCh37
NC_000001.9:g.8340926A>T NCBI36
NG_047035.1:g.464413T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000465125.2:c.2594T>A ENSP00000515651.1:p.Met865Lys
ENST00000400908.7:c.4256T>A MANE Select ENSP00000383700.2:p.Met1419Lys
ENST00000337907.7:c.4256T>A ENSP00000338629.3:p.Met1419Lys
ENST00000377464.5:c.3452T>A ENSP00000366684.1:p.Met1151Lys
ENST00000400907.6:c.1541-2680T>A ENSP00000383699.2:n.1541-2680T>A
ENST00000400908.6:c.4256T>A ENSP00000383700.2:p.Met1419Lys
ENST00000476556.5:c.2594T>A ENSP00000422246.1:p.Met865Lys
ENST00000505225.1:c.308-2033T>A ENSP00000423451.1:n.308-2033T>A
NM_001042681.1:c.4256T>A NP_001036146.1:p.Met1419Lys
NM_001042682.1:c.2594T>A NP_001036147.1:p.Met865Lys
NM_012102.3:c.4256T>A NP_036234.3:p.Met1419Lys
XM_005263464.1:c.4256T>A XP_005263521.1:p.Met1419Lys
XM_005263466.1:c.3452T>A XP_005263523.1:p.Met1151Lys
XM_006710653.1:c.4256T>A XP_006710716.1:p.Met1419Lys
XM_011541510.1:c.4130T>A XP_011539812.1:p.Met1377Lys
XM_005263464.2:c.4256T>A XP_005263521.1:p.Met1419Lys
XM_011541510.2:c.4130T>A XP_011539812.1:p.Met1377Lys
XM_017001358.1:c.4256T>A XP_016856847.1:p.Met1419Lys
XM_017001359.1:c.4256T>A XP_016856848.1:p.Met1419Lys
NM_001042681.2:c.4256T>A MANE Select NP_001036146.1:p.Met1419Lys
NM_001042682.2:c.2594T>A NP_001036147.1:p.Met865Lys
NM_012102.4:c.4256T>A NP_036234.3:p.Met1419Lys