Canonical Allele Identifier: CA1152320932

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8359610_8359613delinsAGAG , CM000663.2:g.8359610_8359613delinsAGAG	GRCh38
NC_000001.10:g.8419670_8419673delinsAGAG , CM000663.1:g.8419670_8419673delinsAGAG	GRCh37
NC_000001.9:g.8342257_8342260delinsAGAG	NCBI36
NG_047035.1:g.463079_463082delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1956+151_1956+154delinsCTCT	ENSP00000515651.1:n.1956+151_1956+154delinsCTCT
ENST00000400908.7:c.3618+151_3618+154delinsCTCT MANE Select	ENSP00000383700.2:n.3618+151_3618+154delinsCTCT
ENST00000337907.7:c.3618+151_3618+154delinsCTCT	ENSP00000338629.3:n.3618+151_3618+154delinsCTCT
ENST00000377464.5:c.2814+151_2814+154delinsCTCT	ENSP00000366684.1:n.2814+151_2814+154delinsCTCT
ENST00000400907.6:c.1541-4014_1541-4011delinsCTCT	ENSP00000383699.2:n.1541-4014_1541-4011delinsCTCT
ENST00000400908.6:c.3618+151_3618+154delinsCTCT	ENSP00000383700.2:n.3618+151_3618+154delinsCTCT
ENST00000476556.5:c.1956+151_1956+154delinsCTCT	ENSP00000422246.1:n.1956+151_1956+154delinsCTCT
ENST00000505225.1:c.307+1847_307+1850delinsCTCT	ENSP00000423451.1:n.307+1847_307+1850delinsCTCT
NM_001042681.1:c.3618+151_3618+154delinsCTCT	NP_001036146.1:n.3618+151_3618+154delinsCTCT
NM_001042682.1:c.1956+151_1956+154delinsCTCT	NP_001036147.1:n.1956+151_1956+154delinsCTCT
NM_012102.3:c.3618+151_3618+154delinsCTCT	NP_036234.3:n.3618+151_3618+154delinsCTCT
XM_005263464.1:c.3618+151_3618+154delinsCTCT	XP_005263521.1:n.3618+151_3618+154delinsCTCT
XM_005263466.1:c.2814+151_2814+154delinsCTCT	XP_005263523.1:n.2814+151_2814+154delinsCTCT
XM_006710653.1:c.3618+151_3618+154delinsCTCT	XP_006710716.1:n.3618+151_3618+154delinsCTCT
XM_011541510.1:c.3492+151_3492+154delinsCTCT	XP_011539812.1:n.3492+151_3492+154delinsCTCT
XM_011541511.1:c.3395+499_3395+502delinsCTCT	XP_011539813.1:n.3395+499_3395+502delinsCTCT
XM_005263464.2:c.3618+151_3618+154delinsCTCT	XP_005263521.1:n.3618+151_3618+154delinsCTCT
XM_011541510.2:c.3492+151_3492+154delinsCTCT	XP_011539812.1:n.3492+151_3492+154delinsCTCT
XM_011541511.2:c.3395+499_3395+502delinsCTCT	XP_011539813.1:n.3395+499_3395+502delinsCTCT
XM_017001358.1:c.3618+151_3618+154delinsCTCT	XP_016856847.1:n.3618+151_3618+154delinsCTCT
XM_017001359.1:c.3618+151_3618+154delinsCTCT	XP_016856848.1:n.3618+151_3618+154delinsCTCT
NM_001042681.2:c.3618+151_3618+154delinsCTCT MANE Select	NP_001036146.1:n.3618+151_3618+154delinsCTCT
NM_001042682.2:c.1956+151_1956+154delinsCTCT	NP_001036147.1:n.1956+151_1956+154delinsCTCT
NM_012102.4:c.3618+151_3618+154delinsCTCT	NP_036234.3:n.3618+151_3618+154delinsCTCT