Canonical Allele Identifier: CA1152436200
Gene: RERE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8699321_8699322delinsCA , CM000663.2:g.8699321_8699322delinsCA GRCh38
NC_000001.10:g.8759380_8759381delinsCA , CM000663.1:g.8759380_8759381delinsCA GRCh37
NC_000001.9:g.8681967_8681968delinsCA NCBI36
NG_047035.1:g.123370_123371delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000704050.1:c.-145+25238_-145+25239delinsTG ENSP00000515653.1:n.-145+25238_-145+25239delinsTG
ENST00000400908.7:c.-144-42881_-144-42880delinsTG MANE Select ENSP00000383700.2:n.-144-42881_-144-42880delinsTG
ENST00000656437.1:c.-144-42881_-144-42880delinsTG ENSP00000499322.1:n.-144-42881_-144-42880delinsTG
ENST00000659924.1:c.-144-42881_-144-42880delinsTG ENSP00000499704.1:n.-144-42881_-144-42880delinsTG
ENST00000337907.7:c.-144-42881_-144-42880delinsTG ENSP00000338629.3:n.-144-42881_-144-42880delinsTG
ENST00000400908.6:c.-144-42881_-144-42880delinsTG ENSP00000383700.2:n.-144-42881_-144-42880delinsTG
ENST00000468247.1:c.-145+3733_-145+3734delinsTG ENSP00000465271.1:n.-145+3733_-145+3734delinsTG
ENST00000480342.5:n.409-42881_409-42880delinsTG
NM_001042681.1:c.-144-42881_-144-42880delinsTG NP_001036146.1:n.-144-42881_-144-42880delinsTG
NM_012102.3:c.-144-42881_-144-42880delinsTG NP_036234.3:n.-144-42881_-144-42880delinsTG
XM_005263464.1:c.-145+3733_-145+3734delinsTG XP_005263521.1:n.-145+3733_-145+3734delinsTG
XM_006710653.1:c.-144-42881_-144-42880delinsTG XP_006710716.1:n.-144-42881_-144-42880delinsTG
XM_011541510.1:c.-144-42881_-144-42880delinsTG XP_011539812.1:n.-144-42881_-144-42880delinsTG
XM_011541511.1:c.-144-42881_-144-42880delinsTG XP_011539813.1:n.-144-42881_-144-42880delinsTG
XM_005263464.2:c.-145+3733_-145+3734delinsTG XP_005263521.1:n.-145+3733_-145+3734delinsTG
XM_011541510.2:c.-144-42881_-144-42880delinsTG XP_011539812.1:n.-144-42881_-144-42880delinsTG
XM_011541511.2:c.-144-42881_-144-42880delinsTG XP_011539813.1:n.-144-42881_-144-42880delinsTG
XM_017001358.1:c.-144-42881_-144-42880delinsTG XP_016856847.1:n.-144-42881_-144-42880delinsTG
XM_017001359.1:c.-145+37561_-145+37562delinsTG XP_016856848.1:n.-145+37561_-145+37562delinsTG
NM_001042681.2:c.-144-42881_-144-42880delinsTG MANE Select NP_001036146.1:n.-144-42881_-144-42880delinsTG
NM_012102.4:c.-144-42881_-144-42880delinsTG NP_036234.3:n.-144-42881_-144-42880delinsTG