Canonical Allele Identifier: CA338171208

Gene: RERE

Linked Data

• MyVariant Identifiers: chr1:g.8420442C>G (hg19) ; chr1:g.8360382C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360382C>G , CM000663.2:g.8360382C>G	GRCh38
NC_000001.10:g.8420442C>G , CM000663.1:g.8420442C>G	GRCh37
NC_000001.9:g.8343029C>G	NCBI36
NG_047035.1:g.462310G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1463G>C	ENSP00000515651.1:p.Gly488Ala
ENST00000400908.7:c.3125G>C MANE Select	ENSP00000383700.2:p.Gly1042Ala
ENST00000337907.7:c.3125G>C	ENSP00000338629.3:p.Gly1042Ala
ENST00000377464.5:c.2321G>C	ENSP00000366684.1:p.Gly774Ala
ENST00000400907.6:c.1540+4364G>C	ENSP00000383699.2:n.1540+4364G>C
ENST00000400908.6:c.3125G>C	ENSP00000383700.2:p.Gly1042Ala
ENST00000476556.5:c.1463G>C	ENSP00000422246.1:p.Gly488Ala
ENST00000505225.1:c.307+1078G>C	ENSP00000423451.1:n.307+1078G>C
NM_001042681.1:c.3125G>C	NP_001036146.1:p.Gly1042Ala
NM_001042682.1:c.1463G>C	NP_001036147.1:p.Gly488Ala
NM_012102.3:c.3125G>C	NP_036234.3:p.Gly1042Ala
XM_005263464.1:c.3125G>C	XP_005263521.1:p.Gly1042Ala
XM_005263466.1:c.2321G>C	XP_005263523.1:p.Gly774Ala
XM_006710653.1:c.3125G>C	XP_006710716.1:p.Gly1042Ala
XM_011541510.1:c.2999G>C	XP_011539812.1:p.Gly1000Ala
XM_011541511.1:c.3125G>C	XP_011539813.1:p.Gly1042Ala
XM_005263464.2:c.3125G>C	XP_005263521.1:p.Gly1042Ala
XM_011541510.2:c.2999G>C	XP_011539812.1:p.Gly1000Ala
XM_011541511.2:c.3125G>C	XP_011539813.1:p.Gly1042Ala
XM_017001358.1:c.3125G>C	XP_016856847.1:p.Gly1042Ala
XM_017001359.1:c.3125G>C	XP_016856848.1:p.Gly1042Ala
NM_001042681.2:c.3125G>C MANE Select	NP_001036146.1:p.Gly1042Ala
NM_001042682.2:c.1463G>C	NP_001036147.1:p.Gly488Ala
NM_012102.4:c.3125G>C	NP_036234.3:p.Gly1042Ala