Canonical Allele Identifier: CA1143940862

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8358341G= , CM000663.2:g.8358341G=	GRCh38
NC_000001.10:g.8418401G= , CM000663.1:g.8418401G=	GRCh37
NC_000001.9:g.8340988G=	NCBI36
NG_047035.1:g.464351C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2532C=	ENSP00000515651.1:p.Ala844=
ENST00000400908.7:c.4194C= MANE Select	ENSP00000383700.2:p.Ala1398=
ENST00000337907.7:c.4194C=	ENSP00000338629.3:p.Ala1398=
ENST00000377464.5:c.3390C=	ENSP00000366684.1:p.Ala1130=
ENST00000400907.6:c.1541-2742C=	ENSP00000383699.2:n.1541-2742C=
ENST00000400908.6:c.4194C=	ENSP00000383700.2:p.Ala1398=
ENST00000476556.5:c.2532C=	ENSP00000422246.1:p.Ala844=
ENST00000505225.1:c.308-2095C=	ENSP00000423451.1:n.308-2095C=
NM_001042681.1:c.4194C=	NP_001036146.1:p.Ala1398=
NM_001042682.1:c.2532C=	NP_001036147.1:p.Ala844=
NM_012102.3:c.4194C=	NP_036234.3:p.Ala1398=
XM_005263464.1:c.4194C=	XP_005263521.1:p.Ala1398=
XM_005263466.1:c.3390C=	XP_005263523.1:p.Ala1130=
XM_006710653.1:c.4194C=	XP_006710716.1:p.Ala1398=
XM_011541510.1:c.4068C=	XP_011539812.1:p.Ala1356=
XM_005263464.2:c.4194C=	XP_005263521.1:p.Ala1398=
XM_011541510.2:c.4068C=	XP_011539812.1:p.Ala1356=
XM_017001358.1:c.4194C=	XP_016856847.1:p.Ala1398=
XM_017001359.1:c.4194C=	XP_016856848.1:p.Ala1398=
NM_001042681.2:c.4194C= MANE Select	NP_001036146.1:p.Ala1398=
NM_001042682.2:c.2532C=	NP_001036147.1:p.Ala844=
NM_012102.4:c.4194C=	NP_036234.3:p.Ala1398=