Canonical Allele Identifier: CA1152436212

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8699361G= , CM000663.2:g.8699361G=	GRCh38
NC_000001.10:g.8759420G= , CM000663.1:g.8759420G=	GRCh37
NC_000001.9:g.8682007G=	NCBI36
NG_047035.1:g.123331C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704050.1:c.-145+25199C=	ENSP00000515653.1:n.-145+25199C=
ENST00000400908.7:c.-144-42920C= MANE Select	ENSP00000383700.2:n.-144-42920C=
ENST00000656437.1:c.-144-42920C=	ENSP00000499322.1:n.-144-42920C=
ENST00000659924.1:c.-144-42920C=	ENSP00000499704.1:n.-144-42920C=
ENST00000337907.7:c.-144-42920C=	ENSP00000338629.3:n.-144-42920C=
ENST00000400908.6:c.-144-42920C=	ENSP00000383700.2:n.-144-42920C=
ENST00000468247.1:c.-145+3694C=	ENSP00000465271.1:n.-145+3694C=
ENST00000480342.5:n.409-42920C=
NM_001042681.1:c.-144-42920C=	NP_001036146.1:n.-144-42920C=
NM_012102.3:c.-144-42920C=	NP_036234.3:n.-144-42920C=
XM_005263464.1:c.-145+3694C=	XP_005263521.1:n.-145+3694C=
XM_006710653.1:c.-144-42920C=	XP_006710716.1:n.-144-42920C=
XM_011541510.1:c.-144-42920C=	XP_011539812.1:n.-144-42920C=
XM_011541511.1:c.-144-42920C=	XP_011539813.1:n.-144-42920C=
XM_005263464.2:c.-145+3694C=	XP_005263521.1:n.-145+3694C=
XM_011541510.2:c.-144-42920C=	XP_011539812.1:n.-144-42920C=
XM_011541511.2:c.-144-42920C=	XP_011539813.1:n.-144-42920C=
XM_017001358.1:c.-144-42920C=	XP_016856847.1:n.-144-42920C=
XM_017001359.1:c.-145+37522C=	XP_016856848.1:n.-145+37522C=
NM_001042681.2:c.-144-42920C= MANE Select	NP_001036146.1:n.-144-42920C=
NM_012102.4:c.-144-42920C=	NP_036234.3:n.-144-42920C=