Canonical Allele Identifier: CA338170952

Gene: RERE

Linked Data

• ClinVar Variation Id: 521884
• ClinVar RCV Id: RCV000624064 ; RCV001839014
• dbSNP Id: rs1259871272
• gnomAD v2: 1-8420302-G-C
• gnomAD v3: 1-8360242-G-C
• gnomAD v4: 1-8360242-G-C
• MyVariant Identifiers: chr1:g.8420302G>C (hg19) ; chr1:g.8360242G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360242G>C , CM000663.2:g.8360242G>C	GRCh38
NC_000001.10:g.8420302G>C , CM000663.1:g.8420302G>C	GRCh37
NC_000001.9:g.8342889G>C	NCBI36
NG_047035.1:g.462450C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1603C>G	ENSP00000515651.1:p.Pro535Ala
ENST00000400908.7:c.3265C>G MANE Select	ENSP00000383700.2:p.Pro1089Ala
ENST00000337907.7:c.3265C>G	ENSP00000338629.3:p.Pro1089Ala
ENST00000377464.5:c.2461C>G	ENSP00000366684.1:p.Pro821Ala
ENST00000400907.6:c.1540+4504C>G	ENSP00000383699.2:n.1540+4504C>G
ENST00000400908.6:c.3265C>G	ENSP00000383700.2:p.Pro1089Ala
ENST00000476556.5:c.1603C>G	ENSP00000422246.1:p.Pro535Ala
ENST00000505225.1:c.307+1218C>G	ENSP00000423451.1:n.307+1218C>G
NM_001042681.1:c.3265C>G	NP_001036146.1:p.Pro1089Ala
NM_001042682.1:c.1603C>G	NP_001036147.1:p.Pro535Ala
NM_012102.3:c.3265C>G	NP_036234.3:p.Pro1089Ala
XM_005263464.1:c.3265C>G	XP_005263521.1:p.Pro1089Ala
XM_005263466.1:c.2461C>G	XP_005263523.1:p.Pro821Ala
XM_006710653.1:c.3265C>G	XP_006710716.1:p.Pro1089Ala
XM_011541510.1:c.3139C>G	XP_011539812.1:p.Pro1047Ala
XM_011541511.1:c.3265C>G	XP_011539813.1:p.Pro1089Ala
XM_005263464.2:c.3265C>G	XP_005263521.1:p.Pro1089Ala
XM_011541510.2:c.3139C>G	XP_011539812.1:p.Pro1047Ala
XM_011541511.2:c.3265C>G	XP_011539813.1:p.Pro1089Ala
XM_017001358.1:c.3265C>G	XP_016856847.1:p.Pro1089Ala
XM_017001359.1:c.3265C>G	XP_016856848.1:p.Pro1089Ala
NM_001042681.2:c.3265C>G MANE Select	NP_001036146.1:p.Pro1089Ala
NM_001042682.2:c.1603C>G	NP_001036147.1:p.Pro535Ala
NM_012102.4:c.3265C>G	NP_036234.3:p.Pro1089Ala