Canonical Allele Identifier: CA571213

Gene: RERE

Linked Data

• ClinVar Variation Id: 2239314
• ClinVar RCV Id: RCV002713957
• dbSNP Id: rs780158112
• ExAC: 1:8420310 C / T
• gnomAD v2: 1-8420310-C-T
• gnomAD v3: 1-8360250-C-T
• gnomAD v4: 1-8360250-C-T
• COSMIC: COSM6428024
• MyVariant Identifiers: chr1:g.8420310C>T (hg19) ; chr1:g.8360250C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360250C>T , CM000663.2:g.8360250C>T	GRCh38
NC_000001.10:g.8420310C>T , CM000663.1:g.8420310C>T	GRCh37
NC_000001.9:g.8342897C>T	NCBI36
NG_047035.1:g.462442G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1595G>A	ENSP00000515651.1:p.Cys532Tyr
ENST00000400908.7:c.3257G>A MANE Select	ENSP00000383700.2:p.Cys1086Tyr
ENST00000337907.7:c.3257G>A	ENSP00000338629.3:p.Cys1086Tyr
ENST00000377464.5:c.2453G>A	ENSP00000366684.1:p.Cys818Tyr
ENST00000400907.6:c.1540+4496G>A	ENSP00000383699.2:n.1540+4496G>A
ENST00000400908.6:c.3257G>A	ENSP00000383700.2:p.Cys1086Tyr
ENST00000476556.5:c.1595G>A	ENSP00000422246.1:p.Cys532Tyr
ENST00000505225.1:c.307+1210G>A	ENSP00000423451.1:n.307+1210G>A
NM_001042681.1:c.3257G>A	NP_001036146.1:p.Cys1086Tyr
NM_001042682.1:c.1595G>A	NP_001036147.1:p.Cys532Tyr
NM_012102.3:c.3257G>A	NP_036234.3:p.Cys1086Tyr
XM_005263464.1:c.3257G>A	XP_005263521.1:p.Cys1086Tyr
XM_005263466.1:c.2453G>A	XP_005263523.1:p.Cys818Tyr
XM_006710653.1:c.3257G>A	XP_006710716.1:p.Cys1086Tyr
XM_011541510.1:c.3131G>A	XP_011539812.1:p.Cys1044Tyr
XM_011541511.1:c.3257G>A	XP_011539813.1:p.Cys1086Tyr
XM_005263464.2:c.3257G>A	XP_005263521.1:p.Cys1086Tyr
XM_011541510.2:c.3131G>A	XP_011539812.1:p.Cys1044Tyr
XM_011541511.2:c.3257G>A	XP_011539813.1:p.Cys1086Tyr
XM_017001358.1:c.3257G>A	XP_016856847.1:p.Cys1086Tyr
XM_017001359.1:c.3257G>A	XP_016856848.1:p.Cys1086Tyr
NM_001042681.2:c.3257G>A MANE Select	NP_001036146.1:p.Cys1086Tyr
NM_001042682.2:c.1595G>A	NP_001036147.1:p.Cys532Tyr
NM_012102.4:c.3257G>A	NP_036234.3:p.Cys1086Tyr