Canonical Allele Identifier: CA570856

Gene: RERE

Linked Data

• ClinVar Variation Id: 2074136
• ClinVar RCV Id: RCV002982145
• dbSNP Id: rs199623549
• ExAC: 1:8418332 G / A
• gnomAD v2: 1-8418332-G-A
• gnomAD v3: 1-8358272-G-A
• gnomAD v4: 1-8358272-G-A
• MyVariant Identifiers: chr1:g.8418332G>A (hg19) ; chr1:g.8358272G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8358272G>A , CM000663.2:g.8358272G>A	GRCh38
NC_000001.10:g.8418332G>A , CM000663.1:g.8418332G>A	GRCh37
NC_000001.9:g.8340919G>A	NCBI36
NG_047035.1:g.464420C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2601C>T	ENSP00000515651.1:p.Asn867=
ENST00000400908.7:c.4263C>T MANE Select	ENSP00000383700.2:p.Asn1421=
ENST00000337907.7:c.4263C>T	ENSP00000338629.3:p.Asn1421=
ENST00000377464.5:c.3459C>T	ENSP00000366684.1:p.Asn1153=
ENST00000400907.6:c.1541-2673C>T	ENSP00000383699.2:n.1541-2673C>T
ENST00000400908.6:c.4263C>T	ENSP00000383700.2:p.Asn1421=
ENST00000476556.5:c.2601C>T	ENSP00000422246.1:p.Asn867=
ENST00000505225.1:c.308-2026C>T	ENSP00000423451.1:n.308-2026C>T
NM_001042681.1:c.4263C>T	NP_001036146.1:p.Asn1421=
NM_001042682.1:c.2601C>T	NP_001036147.1:p.Asn867=
NM_012102.3:c.4263C>T	NP_036234.3:p.Asn1421=
XM_005263464.1:c.4263C>T	XP_005263521.1:p.Asn1421=
XM_005263466.1:c.3459C>T	XP_005263523.1:p.Asn1153=
XM_006710653.1:c.4263C>T	XP_006710716.1:p.Asn1421=
XM_011541510.1:c.4137C>T	XP_011539812.1:p.Asn1379=
XM_005263464.2:c.4263C>T	XP_005263521.1:p.Asn1421=
XM_011541510.2:c.4137C>T	XP_011539812.1:p.Asn1379=
XM_017001358.1:c.4263C>T	XP_016856847.1:p.Asn1421=
XM_017001359.1:c.4263C>T	XP_016856848.1:p.Asn1421=
NM_001042681.2:c.4263C>T MANE Select	NP_001036146.1:p.Asn1421=
NM_001042682.2:c.2601C>T	NP_001036147.1:p.Asn867=
NM_012102.4:c.4263C>T	NP_036234.3:p.Asn1421=