Canonical Allele Identifier: CA415842107

Gene: RERE

Linked Data

• MyVariant Identifiers: chr1:g.8415643A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8355583A>C , CM000663.2:g.8355583A>C	GRCh38
NC_000001.10:g.8415643A>C , CM000663.1:g.8415643A>C	GRCh37
NC_000001.9:g.8338230A>C	NCBI36
NG_047035.1:g.467109T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2841T>G	ENSP00000515651.1:p.Arg947=
ENST00000400908.7:c.4503T>G MANE Select	ENSP00000383700.2:p.Arg1501=
ENST00000337907.7:c.4503T>G	ENSP00000338629.3:p.Arg1501=
ENST00000377464.5:c.3699T>G	ENSP00000366684.1:p.Arg1233=
ENST00000400907.6:c.1557T>G	ENSP00000383699.2:p.Arg519=
ENST00000400908.6:c.4503T>G	ENSP00000383700.2:p.Arg1501=
ENST00000476556.5:c.2841T>G	ENSP00000422246.1:p.Arg947=
ENST00000505225.1:c.471T>G	ENSP00000423451.1:p.Arg157=
NM_001042681.1:c.4503T>G	NP_001036146.1:p.Arg1501=
NM_001042682.1:c.2841T>G	NP_001036147.1:p.Arg947=
NM_012102.3:c.4503T>G	NP_036234.3:p.Arg1501=
XM_005263464.1:c.4503T>G	XP_005263521.1:p.Arg1501=
XM_005263466.1:c.3699T>G	XP_005263523.1:p.Arg1233=
XM_006710653.1:c.4503T>G	XP_006710716.1:p.Arg1501=
XM_011541510.1:c.4377T>G	XP_011539812.1:p.Arg1459=
XM_005263464.2:c.4503T>G	XP_005263521.1:p.Arg1501=
XM_011541510.2:c.4377T>G	XP_011539812.1:p.Arg1459=
XM_017001358.1:c.4503T>G	XP_016856847.1:p.Arg1501=
XM_017001359.1:c.4503T>G	XP_016856848.1:p.Arg1501=
NM_001042681.2:c.4503T>G MANE Select	NP_001036146.1:p.Arg1501=
NM_001042682.2:c.2841T>G	NP_001036147.1:p.Arg947=
NM_012102.4:c.4503T>G	NP_036234.3:p.Arg1501=