Canonical Allele Identifier: CA338168728

Gene: RERE

Linked Data

• ClinVar Variation Id: 985689
• ClinVar RCV Id: RCV001266725
• dbSNP Id: rs1312955446
• MyVariant Identifiers: chr1:g.8418269G>T (hg19) ; chr1:g.8358209G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8358209G>T , CM000663.2:g.8358209G>T	GRCh38
NC_000001.10:g.8418269G>T , CM000663.1:g.8418269G>T	GRCh37
NC_000001.9:g.8340856G>T	NCBI36
NG_047035.1:g.464483C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2664C>A	ENSP00000515651.1:p.Asp888Glu
ENST00000400908.7:c.4326C>A MANE Select	ENSP00000383700.2:p.Asp1442Glu
ENST00000337907.7:c.4326C>A	ENSP00000338629.3:p.Asp1442Glu
ENST00000377464.5:c.3522C>A	ENSP00000366684.1:p.Asp1174Glu
ENST00000400907.6:c.1541-2610C>A	ENSP00000383699.2:n.1541-2610C>A
ENST00000400908.6:c.4326C>A	ENSP00000383700.2:p.Asp1442Glu
ENST00000476556.5:c.2664C>A	ENSP00000422246.1:p.Asp888Glu
ENST00000505225.1:c.308-1963C>A	ENSP00000423451.1:n.308-1963C>A
NM_001042681.1:c.4326C>A	NP_001036146.1:p.Asp1442Glu
NM_001042682.1:c.2664C>A	NP_001036147.1:p.Asp888Glu
NM_012102.3:c.4326C>A	NP_036234.3:p.Asp1442Glu
XM_005263464.1:c.4326C>A	XP_005263521.1:p.Asp1442Glu
XM_005263466.1:c.3522C>A	XP_005263523.1:p.Asp1174Glu
XM_006710653.1:c.4326C>A	XP_006710716.1:p.Asp1442Glu
XM_011541510.1:c.4200C>A	XP_011539812.1:p.Asp1400Glu
XM_005263464.2:c.4326C>A	XP_005263521.1:p.Asp1442Glu
XM_011541510.2:c.4200C>A	XP_011539812.1:p.Asp1400Glu
XM_017001358.1:c.4326C>A	XP_016856847.1:p.Asp1442Glu
XM_017001359.1:c.4326C>A	XP_016856848.1:p.Asp1442Glu
NM_001042681.2:c.4326C>A MANE Select	NP_001036146.1:p.Asp1442Glu
NM_001042682.2:c.2664C>A	NP_001036147.1:p.Asp888Glu
NM_012102.4:c.4326C>A	NP_036234.3:p.Asp1442Glu