Canonical Allele Identifier: CA1152436270
Gene: RERE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.8699496_8699500delinsGGATT , CM000663.2:g.8699496_8699500delinsGGATT GRCh38
NC_000001.10:g.8759555_8759559delinsGGATT , CM000663.1:g.8759555_8759559delinsGGATT GRCh37
NC_000001.9:g.8682142_8682146delinsGGATT NCBI36
NG_047035.1:g.123192_123196delinsAATCC

Transcript Alleles

HGVS Amino-acid change
ENST00000704050.1:c.-145+25060_-145+25064delinsAATCC ENSP00000515653.1:n.-145+25060_-145+25064...
ENST00000400908.7:c.-144-43059_-144-43055delinsAATCC MANE Select ENSP00000383700.2:n.-144-43059_-144-43055...
ENST00000656437.1:c.-144-43059_-144-43055delinsAATCC ENSP00000499322.1:n.-144-43059_-144-43055...
ENST00000659924.1:c.-144-43059_-144-43055delinsAATCC ENSP00000499704.1:n.-144-43059_-144-43055...
ENST00000337907.7:c.-144-43059_-144-43055delinsAATCC ENSP00000338629.3:n.-144-43059_-144-43055...
ENST00000400908.6:c.-144-43059_-144-43055delinsAATCC ENSP00000383700.2:n.-144-43059_-144-43055...
ENST00000468247.1:c.-145+3555_-145+3559delinsAATCC ENSP00000465271.1:n.-145+3555_-145+3559de...
ENST00000480342.5:n.409-43059_409-43055delinsAATCC
NM_001042681.1:c.-144-43059_-144-43055delinsAATCC NP_001036146.1:n.-144-43059_-144-43055del...
NM_012102.3:c.-144-43059_-144-43055delinsAATCC NP_036234.3:n.-144-43059_-144-43055delins...
XM_005263464.1:c.-145+3555_-145+3559delinsAATCC XP_005263521.1:n.-145+3555_-145+3559delin...
XM_006710653.1:c.-144-43059_-144-43055delinsAATCC XP_006710716.1:n.-144-43059_-144-43055del...
XM_011541510.1:c.-144-43059_-144-43055delinsAATCC XP_011539812.1:n.-144-43059_-144-43055del...
XM_011541511.1:c.-144-43059_-144-43055delinsAATCC XP_011539813.1:n.-144-43059_-144-43055del...
XM_005263464.2:c.-145+3555_-145+3559delinsAATCC XP_005263521.1:n.-145+3555_-145+3559delin...
XM_011541510.2:c.-144-43059_-144-43055delinsAATCC XP_011539812.1:n.-144-43059_-144-43055del...
XM_011541511.2:c.-144-43059_-144-43055delinsAATCC XP_011539813.1:n.-144-43059_-144-43055del...
XM_017001358.1:c.-144-43059_-144-43055delinsAATCC XP_016856847.1:n.-144-43059_-144-43055del...
XM_017001359.1:c.-145+37383_-145+37387delinsAATCC XP_016856848.1:n.-145+37383_-145+37387del...
NM_001042681.2:c.-144-43059_-144-43055delinsAATCC MANE Select NP_001036146.1:n.-144-43059_-144-43055del...
NM_012102.4:c.-144-43059_-144-43055delinsAATCC NP_036234.3:n.-144-43059_-144-43055delins...