Canonical Allele Identifier: CA1672873146

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421168_151421171delinsTCAC , CM000668.2:g.151421168_151421171delinsTCAC	GRCh38
NC_000006.11:g.151742303_151742306delinsTCAC , CM000668.1:g.151742303_151742306delinsTCAC	GRCh37
NC_000006.10:g.151783996_151783999delinsTCAC	NCBI36
NG_033031.1:g.36011_36014delinsGTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644054.2:c.*361+74_*361+77delinsGTGA	ENSP00000496328.2:n.*361+74_*361+77delinsGTGA
ENST00000646926.2:c.*39+74_*39+77delinsGTGA	ENSP00000494215.2:n.*39+74_*39+77delinsGTGA
ENST00000682004.1:n.2469+74_2469+77delinsGTGA
ENST00000682299.1:c.1002+1370_1002+1373delinsGTGA	ENSP00000506811.1:n.1002+1370_1002+1373delinsGTGA
ENST00000682392.1:c.1079+74_1079+77delinsGTGA	ENSP00000508314.1:n.1079+74_1079+77delinsGTGA
ENST00000682641.1:c.1079+74_1079+77delinsGTGA	ENSP00000506793.1:n.1079+74_1079+77delinsGTGA
ENST00000683439.1:n.3362+74_3362+77delinsGTGA
ENST00000683724.1:c.1079+74_1079+77delinsGTGA	ENSP00000507984.1:n.1079+74_1079+77delinsGTGA
ENST00000684301.1:c.*478+74_*478+77delinsGTGA	ENSP00000507824.1:n.*478+74_*478+77delinsGTGA
ENST00000684605.1:n.1619+74_1619+77delinsGTGA
ENST00000684658.1:n.1224+74_1224+77delinsGTGA
ENST00000684715.1:n.1224+74_1224+77delinsGTGA
ENST00000684765.1:c.1079+74_1079+77delinsGTGA	ENSP00000507910.1:n.1079+74_1079+77delinsGTGA
ENST00000336451.8:c.*478+74_*478+77delinsGTGA	ENSP00000336683.4:n.*478+74_*478+77delinsGTGA
ENST00000444024.3:c.1079+74_1079+77delinsGTGA MANE Select	ENSP00000412708.2:n.1079+74_1079+77delinsGTGA
ENST00000622845.5:c.569+74_569+77delinsGTGA	ENSP00000481280.1:n.569+74_569+77delinsGTGA
ENST00000644054.1:c.1002+74_1002+77delinsGTGA
ENST00000644711.1:c.1079+74_1079+77delinsGTGA	ENSP00000494106.1:n.1079+74_1079+77delinsGTGA
ENST00000645367.1:n.1131_1134delinsGTGA
ENST00000645895.1:n.1196+74_1196+77delinsGTGA
ENST00000646926.1:c.422+74_422+77delinsGTGA
ENST00000336451.7:c.446+74_446+77delinsGTGA	ENSP00000336683.3:n.446+74_446+77delinsGTGA
ENST00000367303.8:c.1079+74_1079+77delinsGTGA	ENSP00000356272.4:n.1079+74_1079+77delinsGTGA
ENST00000444024.1:c.569+74_569+77delinsGTGA	ENSP00000412708.1:n.569+74_569+77delinsGTGA
ENST00000622845.4:c.569+74_569+77delinsGTGA	ENSP00000481280.1:n.569+74_569+77delinsGTGA
NM_001271937.1:c.569+74_569+77delinsGTGA	NP_001258866.1:n.569+74_569+77delinsGTGA
NM_017909.3:c.1079+74_1079+77delinsGTGA	NP_060379.2:n.1079+74_1079+77delinsGTGA
XM_005267040.2:c.446+74_446+77delinsGTGA	XP_005267097.1:n.446+74_446+77delinsGTGA
XR_942497.1:n.1259+74_1259+77delinsGTGA
XM_005267040.4:c.446+74_446+77delinsGTGA	XP_005267097.1:n.446+74_446+77delinsGTGA
XM_017010988.2:c.446+74_446+77delinsGTGA	XP_016866477.1:n.446+74_446+77delinsGTGA
XR_001743503.2:n.1247+74_1247+77delinsGTGA
XR_002956288.1:n.1204+74_1204+77delinsGTGA
NM_017909.4:c.1079+74_1079+77delinsGTGA MANE Select	NP_060379.2:n.1079+74_1079+77delinsGTGA
NM_001271937.2:c.569+74_569+77delinsGTGA	NP_001258866.1:n.569+74_569+77delinsGTGA