Canonical Allele Identifier: CA338170755

Gene: RERE

Linked Data

• gnomAD v4: 1-8360146-C-T
• MyVariant Identifiers: chr1:g.8420206C>T (hg19) ; chr1:g.8360146C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360146C>T , CM000663.2:g.8360146C>T	GRCh38
NC_000001.10:g.8420206C>T , CM000663.1:g.8420206C>T	GRCh37
NC_000001.9:g.8342793C>T	NCBI36
NG_047035.1:g.462546G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1699G>A	ENSP00000515651.1:p.Val567Met
ENST00000400908.7:c.3361G>A MANE Select	ENSP00000383700.2:p.Val1121Met
ENST00000337907.7:c.3361G>A	ENSP00000338629.3:p.Val1121Met
ENST00000377464.5:c.2557G>A	ENSP00000366684.1:p.Val853Met
ENST00000400907.6:c.1541-4547G>A	ENSP00000383699.2:n.1541-4547G>A
ENST00000400908.6:c.3361G>A	ENSP00000383700.2:p.Val1121Met
ENST00000476556.5:c.1699G>A	ENSP00000422246.1:p.Val567Met
ENST00000505225.1:c.307+1314G>A	ENSP00000423451.1:n.307+1314G>A
NM_001042681.1:c.3361G>A	NP_001036146.1:p.Val1121Met
NM_001042682.1:c.1699G>A	NP_001036147.1:p.Val567Met
NM_012102.3:c.3361G>A	NP_036234.3:p.Val1121Met
XM_005263464.1:c.3361G>A	XP_005263521.1:p.Val1121Met
XM_005263466.1:c.2557G>A	XP_005263523.1:p.Val853Met
XM_006710653.1:c.3361G>A	XP_006710716.1:p.Val1121Met
XM_011541510.1:c.3235G>A	XP_011539812.1:p.Val1079Met
XM_011541511.1:c.3361G>A	XP_011539813.1:p.Val1121Met
XM_005263464.2:c.3361G>A	XP_005263521.1:p.Val1121Met
XM_011541510.2:c.3235G>A	XP_011539812.1:p.Val1079Met
XM_011541511.2:c.3361G>A	XP_011539813.1:p.Val1121Met
XM_017001358.1:c.3361G>A	XP_016856847.1:p.Val1121Met
XM_017001359.1:c.3361G>A	XP_016856848.1:p.Val1121Met
NM_001042681.2:c.3361G>A MANE Select	NP_001036146.1:p.Val1121Met
NM_001042682.2:c.1699G>A	NP_001036147.1:p.Val567Met
NM_012102.4:c.3361G>A	NP_036234.3:p.Val1121Met