Canonical Allele Identifier: CA1672873180

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421247T= , CM000668.2:g.151421247T=	GRCh38
NC_000006.11:g.151742382T= , CM000668.1:g.151742382T=	GRCh37
NC_000006.10:g.151784075T=	NCBI36
NG_033031.1:g.35935A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644054.2:c.*359A=	ENSP00000496328.2:n.*359A=
ENST00000646926.2:c.*37A=	ENSP00000494215.2:n.*37A=
ENST00000682004.1:n.2467A=
ENST00000682299.1:c.1002+1294A=	ENSP00000506811.1:n.1002+1294A=
ENST00000682392.1:c.1077A=	ENSP00000508314.1:p.Leu359=
ENST00000682641.1:c.1077A=	ENSP00000506793.1:p.Leu359=
ENST00000683439.1:n.3360A=
ENST00000683724.1:c.1077A=	ENSP00000507984.1:p.Leu359=
ENST00000684301.1:c.*476A=	ENSP00000507824.1:n.*476A=
ENST00000684605.1:n.1617A=
ENST00000684658.1:n.1222A=
ENST00000684715.1:n.1222A=
ENST00000684765.1:c.1077A=	ENSP00000507910.1:p.Leu359=
ENST00000336451.8:c.*476A=	ENSP00000336683.4:n.*476A=
ENST00000444024.3:c.1077A= MANE Select	ENSP00000412708.2:p.Leu359=
ENST00000622845.5:c.567A=	ENSP00000481280.1:p.Leu189=
ENST00000644054.1:c.1000A=
ENST00000644711.1:c.1077A=	ENSP00000494106.1:p.Leu359=
ENST00000645367.1:n.1055A=
ENST00000645895.1:n.1194A=
ENST00000646926.1:c.420A=
ENST00000336451.7:c.444A=	ENSP00000336683.3:p.Leu148=
ENST00000367303.8:c.1077A=	ENSP00000356272.4:p.Leu359=
ENST00000444024.1:c.567A=	ENSP00000412708.1:p.Leu189=
ENST00000622845.4:c.567A=	ENSP00000481280.1:p.Leu189=
NM_001271937.1:c.567A=	NP_001258866.1:p.Leu189=
NM_017909.3:c.1077A=	NP_060379.2:p.Leu359=
XM_005267040.2:c.444A=	XP_005267097.1:p.Leu148=
XR_942497.1:n.1257A=
XM_005267040.4:c.444A=	XP_005267097.1:p.Leu148=
XM_017010988.2:c.444A=	XP_016866477.1:p.Leu148=
XR_001743503.2:n.1245A=
XR_002956288.1:n.1202A=
NM_017909.4:c.1077A= MANE Select	NP_060379.2:p.Leu359=
NM_001271937.2:c.567A=	NP_001258866.1:p.Leu189=