Canonical Allele Identifier: CA1148423772

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8358170_8358172delinsCCC , CM000663.2:g.8358170_8358172delinsCCC	GRCh38
NC_000001.10:g.8418230_8418232delinsCCC , CM000663.1:g.8418230_8418232delinsCCC	GRCh37
NC_000001.9:g.8340817_8340819delinsCCC	NCBI36
NG_047035.1:g.464520_464522delinsGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2677+24_2677+26delinsGGG	ENSP00000515651.1:n.2677+24_2677+26delinsGGG
ENST00000400908.7:c.4339+24_4339+26delinsGGG MANE Select	ENSP00000383700.2:n.4339+24_4339+26delinsGGG
ENST00000337907.7:c.4339+24_4339+26delinsGGG	ENSP00000338629.3:n.4339+24_4339+26delinsGGG
ENST00000377464.5:c.3535+24_3535+26delinsGGG	ENSP00000366684.1:n.3535+24_3535+26delinsGGG
ENST00000400907.6:c.1541-2573_1541-2571delinsGGG	ENSP00000383699.2:n.1541-2573_1541-2571delinsGGG
ENST00000400908.6:c.4339+24_4339+26delinsGGG	ENSP00000383700.2:n.4339+24_4339+26delinsGGG
ENST00000476556.5:c.2677+24_2677+26delinsGGG	ENSP00000422246.1:n.2677+24_2677+26delinsGGG
ENST00000505225.1:c.308-1926_308-1924delinsGGG	ENSP00000423451.1:n.308-1926_308-1924delinsGGG
NM_001042681.1:c.4339+24_4339+26delinsGGG	NP_001036146.1:n.4339+24_4339+26delinsGGG
NM_001042682.1:c.2677+24_2677+26delinsGGG	NP_001036147.1:n.2677+24_2677+26delinsGGG
NM_012102.3:c.4339+24_4339+26delinsGGG	NP_036234.3:n.4339+24_4339+26delinsGGG
XM_005263464.1:c.4339+24_4339+26delinsGGG	XP_005263521.1:n.4339+24_4339+26delinsGGG
XM_005263466.1:c.3535+24_3535+26delinsGGG	XP_005263523.1:n.3535+24_3535+26delinsGGG
XM_006710653.1:c.4339+24_4339+26delinsGGG	XP_006710716.1:n.4339+24_4339+26delinsGGG
XM_011541510.1:c.4213+24_4213+26delinsGGG	XP_011539812.1:n.4213+24_4213+26delinsGGG
XM_005263464.2:c.4339+24_4339+26delinsGGG	XP_005263521.1:n.4339+24_4339+26delinsGGG
XM_011541510.2:c.4213+24_4213+26delinsGGG	XP_011539812.1:n.4213+24_4213+26delinsGGG
XM_017001358.1:c.4339+24_4339+26delinsGGG	XP_016856847.1:n.4339+24_4339+26delinsGGG
XM_017001359.1:c.4339+24_4339+26delinsGGG	XP_016856848.1:n.4339+24_4339+26delinsGGG
NM_001042681.2:c.4339+24_4339+26delinsGGG MANE Select	NP_001036146.1:n.4339+24_4339+26delinsGGG
NM_001042682.2:c.2677+24_2677+26delinsGGG	NP_001036147.1:n.2677+24_2677+26delinsGGG
NM_012102.4:c.4339+24_4339+26delinsGGG	NP_036234.3:n.4339+24_4339+26delinsGGG