Canonical Allele Identifier: CA416028812

Gene: RERE

Linked Data

• MyVariant Identifiers: chr1:g.8420007G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8359947G>C , CM000663.2:g.8359947G>C	GRCh38
NC_000001.10:g.8420007G>C , CM000663.1:g.8420007G>C	GRCh37
NC_000001.9:g.8342594G>C	NCBI36
NG_047035.1:g.462745C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1773C>G	ENSP00000515651.1:p.Ala591=
ENST00000400908.7:c.3435C>G MANE Select	ENSP00000383700.2:p.Ala1145=
ENST00000337907.7:c.3435C>G	ENSP00000338629.3:p.Ala1145=
ENST00000377464.5:c.2631C>G	ENSP00000366684.1:p.Ala877=
ENST00000400907.6:c.1541-4348C>G	ENSP00000383699.2:n.1541-4348C>G
ENST00000400908.6:c.3435C>G	ENSP00000383700.2:p.Ala1145=
ENST00000476556.5:c.1773C>G	ENSP00000422246.1:p.Ala591=
ENST00000505225.1:c.307+1513C>G	ENSP00000423451.1:n.307+1513C>G
NM_001042681.1:c.3435C>G	NP_001036146.1:p.Ala1145=
NM_001042682.1:c.1773C>G	NP_001036147.1:p.Ala591=
NM_012102.3:c.3435C>G	NP_036234.3:p.Ala1145=
XM_005263464.1:c.3435C>G	XP_005263521.1:p.Ala1145=
XM_005263466.1:c.2631C>G	XP_005263523.1:p.Ala877=
XM_006710653.1:c.3435C>G	XP_006710716.1:p.Ala1145=
XM_011541510.1:c.3309C>G	XP_011539812.1:p.Ala1103=
XM_011541511.1:c.3395+165C>G	XP_011539813.1:n.3395+165C>G
XM_005263464.2:c.3435C>G	XP_005263521.1:p.Ala1145=
XM_011541510.2:c.3309C>G	XP_011539812.1:p.Ala1103=
XM_011541511.2:c.3395+165C>G	XP_011539813.1:n.3395+165C>G
XM_017001358.1:c.3435C>G	XP_016856847.1:p.Ala1145=
XM_017001359.1:c.3435C>G	XP_016856848.1:p.Ala1145=
NM_001042681.2:c.3435C>G MANE Select	NP_001036146.1:p.Ala1145=
NM_001042682.2:c.1773C>G	NP_001036147.1:p.Ala591=
NM_012102.4:c.3435C>G	NP_036234.3:p.Ala1145=