Canonical Allele Identifier: CA571236

Gene: RERE

Linked Data

• dbSNP Id: rs772659157
• ExAC: 1:8420386 C / G
• gnomAD v2: 1-8420386-C-G
• gnomAD v3: 1-8360326-C-G
• gnomAD v4: 1-8360326-C-G
• MyVariant Identifiers: chr1:g.8420386C>G (hg19) ; chr1:g.8360326C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360326C>G , CM000663.2:g.8360326C>G	GRCh38
NC_000001.10:g.8420386C>G , CM000663.1:g.8420386C>G	GRCh37
NC_000001.9:g.8342973C>G	NCBI36
NG_047035.1:g.462366G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1519G>C	ENSP00000515651.1:p.Gly507Arg
ENST00000400908.7:c.3181G>C MANE Select	ENSP00000383700.2:p.Gly1061Arg
ENST00000337907.7:c.3181G>C	ENSP00000338629.3:p.Gly1061Arg
ENST00000377464.5:c.2377G>C	ENSP00000366684.1:p.Gly793Arg
ENST00000400907.6:c.1540+4420G>C	ENSP00000383699.2:n.1540+4420G>C
ENST00000400908.6:c.3181G>C	ENSP00000383700.2:p.Gly1061Arg
ENST00000476556.5:c.1519G>C	ENSP00000422246.1:p.Gly507Arg
ENST00000505225.1:c.307+1134G>C	ENSP00000423451.1:n.307+1134G>C
NM_001042681.1:c.3181G>C	NP_001036146.1:p.Gly1061Arg
NM_001042682.1:c.1519G>C	NP_001036147.1:p.Gly507Arg
NM_012102.3:c.3181G>C	NP_036234.3:p.Gly1061Arg
XM_005263464.1:c.3181G>C	XP_005263521.1:p.Gly1061Arg
XM_005263466.1:c.2377G>C	XP_005263523.1:p.Gly793Arg
XM_006710653.1:c.3181G>C	XP_006710716.1:p.Gly1061Arg
XM_011541510.1:c.3055G>C	XP_011539812.1:p.Gly1019Arg
XM_011541511.1:c.3181G>C	XP_011539813.1:p.Gly1061Arg
XM_005263464.2:c.3181G>C	XP_005263521.1:p.Gly1061Arg
XM_011541510.2:c.3055G>C	XP_011539812.1:p.Gly1019Arg
XM_011541511.2:c.3181G>C	XP_011539813.1:p.Gly1061Arg
XM_017001358.1:c.3181G>C	XP_016856847.1:p.Gly1061Arg
XM_017001359.1:c.3181G>C	XP_016856848.1:p.Gly1061Arg
NM_001042681.2:c.3181G>C MANE Select	NP_001036146.1:p.Gly1061Arg
NM_001042682.2:c.1519G>C	NP_001036147.1:p.Gly507Arg
NM_012102.4:c.3181G>C	NP_036234.3:p.Gly1061Arg