Canonical Allele Identifier: CA1152321334

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360395G= , CM000663.2:g.8360395G=	GRCh38
NC_000001.10:g.8420455G= , CM000663.1:g.8420455G=	GRCh37
NC_000001.9:g.8343042G=	NCBI36
NG_047035.1:g.462297C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1450C=	ENSP00000515651.1:p.Pro484=
ENST00000400908.7:c.3112C= MANE Select	ENSP00000383700.2:p.Pro1038=
ENST00000337907.7:c.3112C=	ENSP00000338629.3:p.Pro1038=
ENST00000377464.5:c.2308C=	ENSP00000366684.1:p.Pro770=
ENST00000400907.6:c.1540+4351C=	ENSP00000383699.2:n.1540+4351C=
ENST00000400908.6:c.3112C=	ENSP00000383700.2:p.Pro1038=
ENST00000476556.5:c.1450C=	ENSP00000422246.1:p.Pro484=
ENST00000505225.1:c.307+1065C=	ENSP00000423451.1:n.307+1065C=
NM_001042681.1:c.3112C=	NP_001036146.1:p.Pro1038=
NM_001042682.1:c.1450C=	NP_001036147.1:p.Pro484=
NM_012102.3:c.3112C=	NP_036234.3:p.Pro1038=
XM_005263464.1:c.3112C=	XP_005263521.1:p.Pro1038=
XM_005263466.1:c.2308C=	XP_005263523.1:p.Pro770=
XM_006710653.1:c.3112C=	XP_006710716.1:p.Pro1038=
XM_011541510.1:c.2986C=	XP_011539812.1:p.Pro996=
XM_011541511.1:c.3112C=	XP_011539813.1:p.Pro1038=
XM_005263464.2:c.3112C=	XP_005263521.1:p.Pro1038=
XM_011541510.2:c.2986C=	XP_011539812.1:p.Pro996=
XM_011541511.2:c.3112C=	XP_011539813.1:p.Pro1038=
XM_017001358.1:c.3112C=	XP_016856847.1:p.Pro1038=
XM_017001359.1:c.3112C=	XP_016856848.1:p.Pro1038=
NM_001042681.2:c.3112C= MANE Select	NP_001036146.1:p.Pro1038=
NM_001042682.2:c.1450C=	NP_001036147.1:p.Pro484=
NM_012102.4:c.3112C=	NP_036234.3:p.Pro1038=