Canonical Allele Identifier: CA571286

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360612G>A , CM000663.2:g.8360612G>A	GRCh38
NC_000001.10:g.8420672G>A , CM000663.1:g.8420672G>A	GRCh37
NC_000001.9:g.8343259G>A	NCBI36
NG_047035.1:g.462080C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001042681.2:c.2895C>T MANE Select	NP_001036146.1:p.Pro965=
ENST00000400908.7:c.2895C>T MANE Select	ENSP00000383700.2:p.Pro965=
NM_001042681.1:c.2895C>T	NP_001036146.1:p.Pro965=
NM_001042682.1:c.1233C>T	NP_001036147.1:p.Pro411=
NM_001042682.2:c.1233C>T	NP_001036147.1:p.Pro411=
NM_012102.3:c.2895C>T	NP_036234.3:p.Pro965=
NM_012102.4:c.2895C>T	NP_036234.3:p.Pro965=
ENST00000337907.7:c.2895C>T	ENSP00000338629.3:p.Pro965=
ENST00000377464.5:c.2091C>T	ENSP00000366684.1:p.Pro697=
ENST00000400907.6:c.1540+4134C>T	ENSP00000383699.2:n.1540+4134C>T
ENST00000400908.6:c.2895C>T	ENSP00000383700.2:p.Pro965=
ENST00000465125.2:c.1233C>T	ENSP00000515651.1:p.Pro411=
ENST00000476556.5:c.1233C>T	ENSP00000422246.1:p.Pro411=
ENST00000505225.1:c.307+848C>T	ENSP00000423451.1:n.307+848C>T
XM_005263464.1:c.2895C>T	XP_005263521.1:p.Pro965=
XM_005263464.2:c.2895C>T	XP_005263521.1:p.Pro965=
XM_005263466.1:c.2091C>T	XP_005263523.1:p.Pro697=
XM_006710653.1:c.2895C>T	XP_006710716.1:p.Pro965=
XM_011541510.1:c.2769C>T	XP_011539812.1:p.Pro923=
XM_011541510.2:c.2769C>T	XP_011539812.1:p.Pro923=
XM_011541511.1:c.2895C>T	XP_011539813.1:p.Pro965=
XM_011541511.2:c.2895C>T	XP_011539813.1:p.Pro965=
XM_017001358.1:c.2895C>T	XP_016856847.1:p.Pro965=
XM_017001359.1:c.2895C>T	XP_016856848.1:p.Pro965=