Canonical Allele Identifier: CA1144092995

Gene: RERE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.8355593G= , CM000663.2:g.8355593G=	GRCh38
NC_000001.10:g.8415653G= , CM000663.1:g.8415653G=	GRCh37
NC_000001.9:g.8338240G=	NCBI36
NG_047035.1:g.467099C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465125.2:c.2831C=	ENSP00000515651.1:p.Pro944=
ENST00000400908.7:c.4493C= MANE Select	ENSP00000383700.2:p.Pro1498=
ENST00000337907.7:c.4493C=	ENSP00000338629.3:p.Pro1498=
ENST00000377464.5:c.3689C=	ENSP00000366684.1:p.Pro1230=
ENST00000400907.6:c.1547C=	ENSP00000383699.2:p.Pro516=
ENST00000400908.6:c.4493C=	ENSP00000383700.2:p.Pro1498=
ENST00000476556.5:c.2831C=	ENSP00000422246.1:p.Pro944=
ENST00000505225.1:c.461C=	ENSP00000423451.1:p.Pro154=
NM_001042681.1:c.4493C=	NP_001036146.1:p.Pro1498=
NM_001042682.1:c.2831C=	NP_001036147.1:p.Pro944=
NM_012102.3:c.4493C=	NP_036234.3:p.Pro1498=
XM_005263464.1:c.4493C=	XP_005263521.1:p.Pro1498=
XM_005263466.1:c.3689C=	XP_005263523.1:p.Pro1230=
XM_006710653.1:c.4493C=	XP_006710716.1:p.Pro1498=
XM_011541510.1:c.4367C=	XP_011539812.1:p.Pro1456=
XM_005263464.2:c.4493C=	XP_005263521.1:p.Pro1498=
XM_011541510.2:c.4367C=	XP_011539812.1:p.Pro1456=
XM_017001358.1:c.4493C=	XP_016856847.1:p.Pro1498=
XM_017001359.1:c.4493C=	XP_016856848.1:p.Pro1498=
NM_001042681.2:c.4493C= MANE Select	NP_001036146.1:p.Pro1498=
NM_001042682.2:c.2831C=	NP_001036147.1:p.Pro944=
NM_012102.4:c.4493C=	NP_036234.3:p.Pro1498=