Canonical Allele Identifier: CA1143435459

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8358200G= , CM000663.2:g.8358200G=	GRCh38
NC_000001.10:g.8418260G= , CM000663.1:g.8418260G=	GRCh37
NC_000001.9:g.8340847G=	NCBI36
NG_047035.1:g.464492C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2673C=	ENSP00000515651.1:p.His891=
ENST00000400908.7:c.4335C= MANE Select	ENSP00000383700.2:p.His1445=
ENST00000337907.7:c.4335C=	ENSP00000338629.3:p.His1445=
ENST00000377464.5:c.3531C=	ENSP00000366684.1:p.His1177=
ENST00000400907.6:c.1541-2601C=	ENSP00000383699.2:n.1541-2601C=
ENST00000400908.6:c.4335C=	ENSP00000383700.2:p.His1445=
ENST00000476556.5:c.2673C=	ENSP00000422246.1:p.His891=
ENST00000505225.1:c.308-1954C=	ENSP00000423451.1:n.308-1954C=
NM_001042681.1:c.4335C=	NP_001036146.1:p.His1445=
NM_001042682.1:c.2673C=	NP_001036147.1:p.His891=
NM_012102.3:c.4335C=	NP_036234.3:p.His1445=
XM_005263464.1:c.4335C=	XP_005263521.1:p.His1445=
XM_005263466.1:c.3531C=	XP_005263523.1:p.His1177=
XM_006710653.1:c.4335C=	XP_006710716.1:p.His1445=
XM_011541510.1:c.4209C=	XP_011539812.1:p.His1403=
XM_005263464.2:c.4335C=	XP_005263521.1:p.His1445=
XM_011541510.2:c.4209C=	XP_011539812.1:p.His1403=
XM_017001358.1:c.4335C=	XP_016856847.1:p.His1445=
XM_017001359.1:c.4335C=	XP_016856848.1:p.His1445=
NM_001042681.2:c.4335C= MANE Select	NP_001036146.1:p.His1445=
NM_001042682.2:c.2673C=	NP_001036147.1:p.His891=
NM_012102.4:c.4335C=	NP_036234.3:p.His1445=