Canonical Allele Identifier: CA293085

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151405236C>T , CM000668.2:g.151405236C>T	GRCh38
NC_000006.11:g.151726371C>T , CM000668.1:g.151726371C>T	GRCh37
NC_000006.10:g.151768064C>T	NCBI36
NG_033031.1:g.51946G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646926.2:c.*309G>A	ENSP00000494215.2:n.*309G>A
ENST00000682004.1:n.2739G>A
ENST00000682299.1:c.1151G>A	ENSP00000506811.1:p.Ter384=
ENST00000682392.1:c.*150G>A	ENSP00000508314.1:n.*150G>A
ENST00000682641.1:c.1317+484G>A	ENSP00000506793.1:n.1317+484G>A
ENST00000683439.1:n.3632G>A
ENST00000683724.1:c.1349G>A	ENSP00000507984.1:p.Ter450=
ENST00000684301.1:c.*821G>A	ENSP00000507824.1:n.*821G>A
ENST00000684605.1:n.1889G>A
ENST00000684765.1:c.*277G>A	ENSP00000507910.1:n.*277G>A
ENST00000336451.8:c.*748G>A	ENSP00000336683.4:n.*748G>A
ENST00000444024.3:c.1349G>A MANE Select	ENSP00000412708.2:p.Ter450=
ENST00000622845.5:c.839G>A	ENSP00000481280.1:p.Ter280=
ENST00000644711.1:c.*272G>A	ENSP00000494106.1:n.*272G>A
ENST00000646926.1:c.692G>A
ENST00000336451.7:c.716G>A	ENSP00000336683.3:p.Ter239=
ENST00000367303.8:c.1349G>A	ENSP00000356272.4:p.Ter450=
ENST00000622845.4:c.839G>A	ENSP00000481280.1:p.Ter280=
NM_001271937.1:c.839G>A	NP_001258866.1:p.Ter280=
NM_017909.3:c.1349G>A	NP_060379.2:p.Ter450=
XM_005267040.2:c.716G>A	XP_005267097.1:p.Ter239=
XR_942497.1:n.1787G>A
XM_005267040.4:c.716G>A	XP_005267097.1:p.Ter239=
XM_017010988.2:c.716G>A	XP_016866477.1:p.Ter239=
XR_001743503.2:n.1517G>A
XR_002956288.1:n.1732G>A
NM_017909.4:c.1349G>A MANE Select	NP_060379.2:p.Ter450=
NM_001271937.2:c.839G>A	NP_001258866.1:p.Ter280=