Canonical Allele Identifier: CA338168336

Gene: RERE

Linked Data

• gnomAD v4: 1-8355582-C-A
• MyVariant Identifiers: chr1:g.8415642C>A (hg19) ; chr1:g.8355582C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8355582C>A , CM000663.2:g.8355582C>A	GRCh38
NC_000001.10:g.8415642C>A , CM000663.1:g.8415642C>A	GRCh37
NC_000001.9:g.8338229C>A	NCBI36
NG_047035.1:g.467110G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2842G>T	ENSP00000515651.1:p.Asp948Tyr
ENST00000400908.7:c.4504G>T MANE Select	ENSP00000383700.2:p.Asp1502Tyr
ENST00000337907.7:c.4504G>T	ENSP00000338629.3:p.Asp1502Tyr
ENST00000377464.5:c.3700G>T	ENSP00000366684.1:p.Asp1234Tyr
ENST00000400907.6:c.1558G>T	ENSP00000383699.2:p.Asp520Tyr
ENST00000400908.6:c.4504G>T	ENSP00000383700.2:p.Asp1502Tyr
ENST00000476556.5:c.2842G>T	ENSP00000422246.1:p.Asp948Tyr
ENST00000505225.1:c.472G>T	ENSP00000423451.1:p.Asp158Tyr
NM_001042681.1:c.4504G>T	NP_001036146.1:p.Asp1502Tyr
NM_001042682.1:c.2842G>T	NP_001036147.1:p.Asp948Tyr
NM_012102.3:c.4504G>T	NP_036234.3:p.Asp1502Tyr
XM_005263464.1:c.4504G>T	XP_005263521.1:p.Asp1502Tyr
XM_005263466.1:c.3700G>T	XP_005263523.1:p.Asp1234Tyr
XM_006710653.1:c.4504G>T	XP_006710716.1:p.Asp1502Tyr
XM_011541510.1:c.4378G>T	XP_011539812.1:p.Asp1460Tyr
XM_005263464.2:c.4504G>T	XP_005263521.1:p.Asp1502Tyr
XM_011541510.2:c.4378G>T	XP_011539812.1:p.Asp1460Tyr
XM_017001358.1:c.4504G>T	XP_016856847.1:p.Asp1502Tyr
XM_017001359.1:c.4504G>T	XP_016856848.1:p.Asp1502Tyr
NM_001042681.2:c.4504G>T MANE Select	NP_001036146.1:p.Asp1502Tyr
NM_001042682.2:c.2842G>T	NP_001036147.1:p.Asp948Tyr
NM_012102.4:c.4504G>T	NP_036234.3:p.Asp1502Tyr