Canonical Allele Identifier: CA2643072815

Gene: RERE

Linked Data

• gnomAD v4: 1-8355378-C-CTCAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8355380_8355384dup , CM000663.2:g.8355380_8355384dup	GRCh38
NC_000001.10:g.8415440_8415444dup , CM000663.1:g.8415440_8415444dup	GRCh37
NC_000001.9:g.8338027_8338031dup	NCBI36
NG_047035.1:g.467309_467313dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.3005+36_3005+40dup	ENSP00000515651.1:n.3005+36_3005+40dup
ENST00000400908.7:c.4667+36_4667+40dup MANE Select	ENSP00000383700.2:n.4667+36_4667+40dup
ENST00000337907.7:c.4667+36_4667+40dup	ENSP00000338629.3:n.4667+36_4667+40dup
ENST00000377464.5:c.3863+36_3863+40dup	ENSP00000366684.1:n.3863+36_3863+40dup
ENST00000400907.6:c.1721+36_1721+40dup	ENSP00000383699.2:n.1721+36_1721+40dup
ENST00000400908.6:c.4667+36_4667+40dup	ENSP00000383700.2:n.4667+36_4667+40dup
ENST00000476556.5:c.3005+36_3005+40dup	ENSP00000422246.1:n.3005+36_3005+40dup
NM_001042681.1:c.4667+36_4667+40dup	NP_001036146.1:n.4667+36_4667+40dup
NM_001042682.1:c.3005+36_3005+40dup	NP_001036147.1:n.3005+36_3005+40dup
NM_012102.3:c.4667+36_4667+40dup	NP_036234.3:n.4667+36_4667+40dup
XM_005263464.1:c.4667+36_4667+40dup	XP_005263521.1:n.4667+36_4667+40dup
XM_005263466.1:c.3863+36_3863+40dup	XP_005263523.1:n.3863+36_3863+40dup
XM_006710653.1:c.4667+36_4667+40dup	XP_006710716.1:n.4667+36_4667+40dup
XM_011541510.1:c.4541+36_4541+40dup	XP_011539812.1:n.4541+36_4541+40dup
XM_005263464.2:c.4667+36_4667+40dup	XP_005263521.1:n.4667+36_4667+40dup
XM_011541510.2:c.4541+36_4541+40dup	XP_011539812.1:n.4541+36_4541+40dup
XM_017001358.1:c.4667+36_4667+40dup	XP_016856847.1:n.4667+36_4667+40dup
XM_017001359.1:c.4667+36_4667+40dup	XP_016856848.1:n.4667+36_4667+40dup
NM_001042681.2:c.4667+36_4667+40dup MANE Select	NP_001036146.1:n.4667+36_4667+40dup
NM_001042682.2:c.3005+36_3005+40dup	NP_001036147.1:n.3005+36_3005+40dup
NM_012102.4:c.4667+36_4667+40dup	NP_036234.3:n.4667+36_4667+40dup