Canonical Allele Identifier: CA570854

Gene: RERE

Linked Data

• ClinVar Variation Id: 2413233
• ClinVar RCV Id: RCV003110236
• dbSNP Id: rs753600821
• ExAC: 1:8418326 A / G
• gnomAD v2: 1-8418326-A-G
• gnomAD v3: 1-8358266-A-G
• gnomAD v4: 1-8358266-A-G
• MyVariant Identifiers: chr1:g.8418326A>G (hg19) ; chr1:g.8358266A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8358266A>G , CM000663.2:g.8358266A>G	GRCh38
NC_000001.10:g.8418326A>G , CM000663.1:g.8418326A>G	GRCh37
NC_000001.9:g.8340913A>G	NCBI36
NG_047035.1:g.464426T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2607T>C	ENSP00000515651.1:p.Thr869=
ENST00000400908.7:c.4269T>C MANE Select	ENSP00000383700.2:p.Thr1423=
ENST00000337907.7:c.4269T>C	ENSP00000338629.3:p.Thr1423=
ENST00000377464.5:c.3465T>C	ENSP00000366684.1:p.Thr1155=
ENST00000400907.6:c.1541-2667T>C	ENSP00000383699.2:n.1541-2667T>C
ENST00000400908.6:c.4269T>C	ENSP00000383700.2:p.Thr1423=
ENST00000476556.5:c.2607T>C	ENSP00000422246.1:p.Thr869=
ENST00000505225.1:c.308-2020T>C	ENSP00000423451.1:n.308-2020T>C
NM_001042681.1:c.4269T>C	NP_001036146.1:p.Thr1423=
NM_001042682.1:c.2607T>C	NP_001036147.1:p.Thr869=
NM_012102.3:c.4269T>C	NP_036234.3:p.Thr1423=
XM_005263464.1:c.4269T>C	XP_005263521.1:p.Thr1423=
XM_005263466.1:c.3465T>C	XP_005263523.1:p.Thr1155=
XM_006710653.1:c.4269T>C	XP_006710716.1:p.Thr1423=
XM_011541510.1:c.4143T>C	XP_011539812.1:p.Thr1381=
XM_005263464.2:c.4269T>C	XP_005263521.1:p.Thr1423=
XM_011541510.2:c.4143T>C	XP_011539812.1:p.Thr1381=
XM_017001358.1:c.4269T>C	XP_016856847.1:p.Thr1423=
XM_017001359.1:c.4269T>C	XP_016856848.1:p.Thr1423=
NM_001042681.2:c.4269T>C MANE Select	NP_001036146.1:p.Thr1423=
NM_001042682.2:c.2607T>C	NP_001036147.1:p.Thr869=
NM_012102.4:c.4269T>C	NP_036234.3:p.Thr1423=