Canonical Allele Identifier: CA1143906286

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8359917G= , CM000663.2:g.8359917G=	GRCh38
NC_000001.10:g.8419977G= , CM000663.1:g.8419977G=	GRCh37
NC_000001.9:g.8342564G=	NCBI36
NG_047035.1:g.462775C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1803C=	ENSP00000515651.1:p.Ala601=
ENST00000400908.7:c.3465C= MANE Select	ENSP00000383700.2:p.Ala1155=
ENST00000337907.7:c.3465C=	ENSP00000338629.3:p.Ala1155=
ENST00000377464.5:c.2661C=	ENSP00000366684.1:p.Ala887=
ENST00000400907.6:c.1541-4318C=	ENSP00000383699.2:n.1541-4318C=
ENST00000400908.6:c.3465C=	ENSP00000383700.2:p.Ala1155=
ENST00000476556.5:c.1803C=	ENSP00000422246.1:p.Ala601=
ENST00000505225.1:c.307+1543C=	ENSP00000423451.1:n.307+1543C=
NM_001042681.1:c.3465C=	NP_001036146.1:p.Ala1155=
NM_001042682.1:c.1803C=	NP_001036147.1:p.Ala601=
NM_012102.3:c.3465C=	NP_036234.3:p.Ala1155=
XM_005263464.1:c.3465C=	XP_005263521.1:p.Ala1155=
XM_005263466.1:c.2661C=	XP_005263523.1:p.Ala887=
XM_006710653.1:c.3465C=	XP_006710716.1:p.Ala1155=
XM_011541510.1:c.3339C=	XP_011539812.1:p.Ala1113=
XM_011541511.1:c.3395+195C=	XP_011539813.1:n.3395+195C=
XM_005263464.2:c.3465C=	XP_005263521.1:p.Ala1155=
XM_011541510.2:c.3339C=	XP_011539812.1:p.Ala1113=
XM_011541511.2:c.3395+195C=	XP_011539813.1:n.3395+195C=
XM_017001358.1:c.3465C=	XP_016856847.1:p.Ala1155=
XM_017001359.1:c.3465C=	XP_016856848.1:p.Ala1155=
NM_001042681.2:c.3465C= MANE Select	NP_001036146.1:p.Ala1155=
NM_001042682.2:c.1803C=	NP_001036147.1:p.Ala601=
NM_012102.4:c.3465C=	NP_036234.3:p.Ala1155=