Canonical Allele Identifier: CA1152321339

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8360406A= , CM000663.2:g.8360406A=	GRCh38
NC_000001.10:g.8420466A= , CM000663.1:g.8420466A=	GRCh37
NC_000001.9:g.8343053A=	NCBI36
NG_047035.1:g.462286T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.1439T=	ENSP00000515651.1:p.Phe480=
ENST00000400908.7:c.3101T= MANE Select	ENSP00000383700.2:p.Phe1034=
ENST00000337907.7:c.3101T=	ENSP00000338629.3:p.Phe1034=
ENST00000377464.5:c.2297T=	ENSP00000366684.1:p.Phe766=
ENST00000400907.6:c.1540+4340T=	ENSP00000383699.2:n.1540+4340T=
ENST00000400908.6:c.3101T=	ENSP00000383700.2:p.Phe1034=
ENST00000476556.5:c.1439T=	ENSP00000422246.1:p.Phe480=
ENST00000505225.1:c.307+1054T=	ENSP00000423451.1:n.307+1054T=
NM_001042681.1:c.3101T=	NP_001036146.1:p.Phe1034=
NM_001042682.1:c.1439T=	NP_001036147.1:p.Phe480=
NM_012102.3:c.3101T=	NP_036234.3:p.Phe1034=
XM_005263464.1:c.3101T=	XP_005263521.1:p.Phe1034=
XM_005263466.1:c.2297T=	XP_005263523.1:p.Phe766=
XM_006710653.1:c.3101T=	XP_006710716.1:p.Phe1034=
XM_011541510.1:c.2975T=	XP_011539812.1:p.Phe992=
XM_011541511.1:c.3101T=	XP_011539813.1:p.Phe1034=
XM_005263464.2:c.3101T=	XP_005263521.1:p.Phe1034=
XM_011541510.2:c.2975T=	XP_011539812.1:p.Phe992=
XM_011541511.2:c.3101T=	XP_011539813.1:p.Phe1034=
XM_017001358.1:c.3101T=	XP_016856847.1:p.Phe1034=
XM_017001359.1:c.3101T=	XP_016856848.1:p.Phe1034=
NM_001042681.2:c.3101T= MANE Select	NP_001036146.1:p.Phe1034=
NM_001042682.2:c.1439T=	NP_001036147.1:p.Phe480=
NM_012102.4:c.3101T=	NP_036234.3:p.Phe1034=