Canonical Allele Identifier: CA570729

Gene: RERE

Linked Data

• ClinVar Variation Id: 1636478
• ClinVar RCV Id: RCV002135482
• dbSNP Id: rs148510143
• ExAC: 1:8415508 G / A
• gnomAD v2: 1-8415508-G-A
• gnomAD v3: 1-8355448-G-A
• gnomAD v4: 1-8355448-G-A
• MyVariant Identifiers: chr1:g.8415508G>A (hg19) ; chr1:g.8355448G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8355448G>A , CM000663.2:g.8355448G>A	GRCh38
NC_000001.10:g.8415508G>A , CM000663.1:g.8415508G>A	GRCh37
NC_000001.9:g.8338095G>A	NCBI36
NG_047035.1:g.467244C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2976C>T	ENSP00000515651.1:p.Gly992=
ENST00000400908.7:c.4638C>T MANE Select	ENSP00000383700.2:p.Gly1546=
ENST00000337907.7:c.4638C>T	ENSP00000338629.3:p.Gly1546=
ENST00000377464.5:c.3834C>T	ENSP00000366684.1:p.Gly1278=
ENST00000400907.6:c.1692C>T	ENSP00000383699.2:p.Gly564=
ENST00000400908.6:c.4638C>T	ENSP00000383700.2:p.Gly1546=
ENST00000476556.5:c.2976C>T	ENSP00000422246.1:p.Gly992=
NM_001042681.1:c.4638C>T	NP_001036146.1:p.Gly1546=
NM_001042682.1:c.2976C>T	NP_001036147.1:p.Gly992=
NM_012102.3:c.4638C>T	NP_036234.3:p.Gly1546=
XM_005263464.1:c.4638C>T	XP_005263521.1:p.Gly1546=
XM_005263466.1:c.3834C>T	XP_005263523.1:p.Gly1278=
XM_006710653.1:c.4638C>T	XP_006710716.1:p.Gly1546=
XM_011541510.1:c.4512C>T	XP_011539812.1:p.Gly1504=
XM_005263464.2:c.4638C>T	XP_005263521.1:p.Gly1546=
XM_011541510.2:c.4512C>T	XP_011539812.1:p.Gly1504=
XM_017001358.1:c.4638C>T	XP_016856847.1:p.Gly1546=
XM_017001359.1:c.4638C>T	XP_016856848.1:p.Gly1546=
NM_001042681.2:c.4638C>T MANE Select	NP_001036146.1:p.Gly1546=
NM_001042682.2:c.2976C>T	NP_001036147.1:p.Gly992=
NM_012102.4:c.4638C>T	NP_036234.3:p.Gly1546=