Canonical Allele Identifier: CA1152320990

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8359696_8359724delinsCCCAGCGTGGCTCCCAGGCGCAGGATGGA , CM000663.2:g.8359696_8359724delinsCCCAGCGTGGCTCCCAGGCGCAGGATGGA	GRCh38
NC_000001.10:g.8419756_8419784delinsCCCAGCGTGGCTCCCAGGCGCAGGATGGA , CM000663.1:g.8419756_8419784delinsCCCAGCGTGGCTCCCAGGCGCAGGATGGA	GRCh37
NC_000001.9:g.8342343_8342371delinsCCCAGCGTGGCTCCCAGGCGCAGGATGGA	NCBI36
NG_047035.1:g.462968_462996delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	ENSP00000515651.1:n.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGC...
ENST00000400908.7:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG MANE Select	ENSP00000383700.2:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGC...
ENST00000337907.7:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	ENSP00000338629.3:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGC...
ENST00000377464.5:c.2814+40_2814+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	ENSP00000366684.1:n.2814+40_2814+68delinsTCCATCCTGCGCCTGGGAGC...
ENST00000400907.6:c.1541-4125_1541-4097delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	ENSP00000383699.2:n.1541-4125_1541-4097delinsTCCATCCTGCGCCTGG...
ENST00000400908.6:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	ENSP00000383700.2:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGC...
ENST00000476556.5:c.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	ENSP00000422246.1:n.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGC...
ENST00000505225.1:c.307+1736_307+1764delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	ENSP00000423451.1:n.307+1736_307+1764delinsTCCATCCTGCGCCTGGGA...
NM_001042681.1:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	NP_001036146.1:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCAC...
NM_001042682.1:c.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	NP_001036147.1:n.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGCCAC...
NM_012102.3:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	NP_036234.3:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCT...
XM_005263464.1:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_005263521.1:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCAC...
XM_005263466.1:c.2814+40_2814+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_005263523.1:n.2814+40_2814+68delinsTCCATCCTGCGCCTGGGAGCCAC...
XM_006710653.1:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_006710716.1:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCAC...
XM_011541510.1:c.3492+40_3492+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_011539812.1:n.3492+40_3492+68delinsTCCATCCTGCGCCTGGGAGCCAC...
XM_011541511.1:c.3395+388_3395+416delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_011539813.1:n.3395+388_3395+416delinsTCCATCCTGCGCCTGGGAGCC...
XM_005263464.2:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_005263521.1:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCAC...
XM_011541510.2:c.3492+40_3492+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_011539812.1:n.3492+40_3492+68delinsTCCATCCTGCGCCTGGGAGCCAC...
XM_011541511.2:c.3395+388_3395+416delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_011539813.1:n.3395+388_3395+416delinsTCCATCCTGCGCCTGGGAGCC...
XM_017001358.1:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_016856847.1:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCAC...
XM_017001359.1:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	XP_016856848.1:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCAC...
NM_001042681.2:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG MANE Select	NP_001036146.1:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCAC...
NM_001042682.2:c.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	NP_001036147.1:n.1956+40_1956+68delinsTCCATCCTGCGCCTGGGAGCCAC...
NM_012102.4:c.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCTGGG	NP_036234.3:n.3618+40_3618+68delinsTCCATCCTGCGCCTGGGAGCCACGCT...