Canonical Allele Identifier: CA1140046900

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8466082G= , CM000663.2:g.8466082G=	GRCh38
NC_000001.10:g.8526142G= , CM000663.1:g.8526142G=	GRCh37
NC_000001.9:g.8448729G=	NCBI36
NG_047035.1:g.356610C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001042681.2:c.1105-59C= MANE Select	NP_001036146.1:n.1105-59C=
ENST00000400908.7:c.1105-59C= MANE Select	ENSP00000383700.2:n.1105-59C=
NM_001042681.1:c.1105-59C=	NP_001036146.1:n.1105-59C=
NM_012102.3:c.1105-59C=	NP_036234.3:n.1105-59C=
NM_012102.4:c.1105-59C=	NP_036234.3:n.1105-59C=
ENST00000337907.7:c.1105-59C=	ENSP00000338629.3:n.1105-59C=
ENST00000377464.5:c.301-59C=	ENSP00000366684.1:n.301-59C=
ENST00000400907.6:c.1105-59C=	ENSP00000383699.2:n.1105-59C=
ENST00000400908.6:c.1105-59C=	ENSP00000383700.2:n.1105-59C=
ENST00000464972.5:c.151-59C=	ENSP00000464712.1:n.151-59C=
ENST00000480342.5:n.1657-59C=
ENST00000656437.1:c.1105-59C=	ENSP00000499322.1:n.1105-59C=
ENST00000659924.1:c.1105-59C=	ENSP00000499704.1:n.1105-59C=
ENST00000704049.1:c.301-59C=	ENSP00000515652.1:n.301-59C=
XM_005263464.1:c.1105-59C=	XP_005263521.1:n.1105-59C=
XM_005263464.2:c.1105-59C=	XP_005263521.1:n.1105-59C=
XM_005263466.1:c.301-59C=	XP_005263523.1:n.301-59C=
XM_006710653.1:c.1105-59C=	XP_006710716.1:n.1105-59C=
XM_011541510.1:c.979-59C=	XP_011539812.1:n.979-59C=
XM_011541510.2:c.979-59C=	XP_011539812.1:n.979-59C=
XM_011541511.1:c.1105-59C=	XP_011539813.1:n.1105-59C=
XM_011541511.2:c.1105-59C=	XP_011539813.1:n.1105-59C=
XM_017001358.1:c.1105-59C=	XP_016856847.1:n.1105-59C=
XM_017001359.1:c.1105-59C=	XP_016856848.1:n.1105-59C=