Canonical Allele Identifier: CA338168181

Gene: RERE

Linked Data

• MyVariant Identifiers: chr1:g.8415568C>G (hg19) ; chr1:g.8355508C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8355508C>G , CM000663.2:g.8355508C>G	GRCh38
NC_000001.10:g.8415568C>G , CM000663.1:g.8415568C>G	GRCh37
NC_000001.9:g.8338155C>G	NCBI36
NG_047035.1:g.467184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2916G>C	ENSP00000515651.1:p.Glu972Asp
ENST00000400908.7:c.4578G>C MANE Select	ENSP00000383700.2:p.Glu1526Asp
ENST00000337907.7:c.4578G>C	ENSP00000338629.3:p.Glu1526Asp
ENST00000377464.5:c.3774G>C	ENSP00000366684.1:p.Glu1258Asp
ENST00000400907.6:c.1632G>C	ENSP00000383699.2:p.Glu544Asp
ENST00000400908.6:c.4578G>C	ENSP00000383700.2:p.Glu1526Asp
ENST00000476556.5:c.2916G>C	ENSP00000422246.1:p.Glu972Asp
NM_001042681.1:c.4578G>C	NP_001036146.1:p.Glu1526Asp
NM_001042682.1:c.2916G>C	NP_001036147.1:p.Glu972Asp
NM_012102.3:c.4578G>C	NP_036234.3:p.Glu1526Asp
XM_005263464.1:c.4578G>C	XP_005263521.1:p.Glu1526Asp
XM_005263466.1:c.3774G>C	XP_005263523.1:p.Glu1258Asp
XM_006710653.1:c.4578G>C	XP_006710716.1:p.Glu1526Asp
XM_011541510.1:c.4452G>C	XP_011539812.1:p.Glu1484Asp
XM_005263464.2:c.4578G>C	XP_005263521.1:p.Glu1526Asp
XM_011541510.2:c.4452G>C	XP_011539812.1:p.Glu1484Asp
XM_017001358.1:c.4578G>C	XP_016856847.1:p.Glu1526Asp
XM_017001359.1:c.4578G>C	XP_016856848.1:p.Glu1526Asp
NM_001042681.2:c.4578G>C MANE Select	NP_001036146.1:p.Glu1526Asp
NM_001042682.2:c.2916G>C	NP_001036147.1:p.Glu972Asp
NM_012102.4:c.4578G>C	NP_036234.3:p.Glu1526Asp