Canonical Allele Identifier: CA571182

Gene: RERE

Linked Data

• ClinVar Variation Id: 3153015
• ClinVar RCV Id: RCV004445916
• dbSNP Id: rs566753880
• ExAC: 1:8420199 G / T
• gnomAD v2: 1-8420199-G-T
• gnomAD v3: 1-8360139-G-T
• gnomAD v4: 1-8360139-G-T
• MyVariant Identifiers: chr1:g.8420199G>T (hg19) ; chr1:g.8360139G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360139G>T , CM000663.2:g.8360139G>T	GRCh38
NC_000001.10:g.8420199G>T , CM000663.1:g.8420199G>T	GRCh37
NC_000001.9:g.8342786G>T	NCBI36
NG_047035.1:g.462553C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1706C>A	ENSP00000515651.1:p.Thr569Asn
ENST00000400908.7:c.3368C>A MANE Select	ENSP00000383700.2:p.Thr1123Asn
ENST00000337907.7:c.3368C>A	ENSP00000338629.3:p.Thr1123Asn
ENST00000377464.5:c.2564C>A	ENSP00000366684.1:p.Thr855Asn
ENST00000400907.6:c.1541-4540C>A	ENSP00000383699.2:n.1541-4540C>A
ENST00000400908.6:c.3368C>A	ENSP00000383700.2:p.Thr1123Asn
ENST00000476556.5:c.1706C>A	ENSP00000422246.1:p.Thr569Asn
ENST00000505225.1:c.307+1321C>A	ENSP00000423451.1:n.307+1321C>A
NM_001042681.1:c.3368C>A	NP_001036146.1:p.Thr1123Asn
NM_001042682.1:c.1706C>A	NP_001036147.1:p.Thr569Asn
NM_012102.3:c.3368C>A	NP_036234.3:p.Thr1123Asn
XM_005263464.1:c.3368C>A	XP_005263521.1:p.Thr1123Asn
XM_005263466.1:c.2564C>A	XP_005263523.1:p.Thr855Asn
XM_006710653.1:c.3368C>A	XP_006710716.1:p.Thr1123Asn
XM_011541510.1:c.3242C>A	XP_011539812.1:p.Thr1081Asn
XM_011541511.1:c.3368C>A	XP_011539813.1:p.Thr1123Asn
XM_005263464.2:c.3368C>A	XP_005263521.1:p.Thr1123Asn
XM_011541510.2:c.3242C>A	XP_011539812.1:p.Thr1081Asn
XM_011541511.2:c.3368C>A	XP_011539813.1:p.Thr1123Asn
XM_017001358.1:c.3368C>A	XP_016856847.1:p.Thr1123Asn
XM_017001359.1:c.3368C>A	XP_016856848.1:p.Thr1123Asn
NM_001042681.2:c.3368C>A MANE Select	NP_001036146.1:p.Thr1123Asn
NM_001042682.2:c.1706C>A	NP_001036147.1:p.Thr569Asn
NM_012102.4:c.3368C>A	NP_036234.3:p.Thr1123Asn