Canonical Allele Identifier: CA1672873177

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421231_151421235delinsGAGAA , CM000668.2:g.151421231_151421235delinsGAGAA	GRCh38
NC_000006.11:g.151742366_151742370delinsGAGAA , CM000668.1:g.151742366_151742370delinsGAGAA	GRCh37
NC_000006.10:g.151784059_151784063delinsGAGAA	NCBI36
NG_033031.1:g.35947_35951delinsTTCTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000644054.2:c.*361+10_*361+14delinsTTCTC	ENSP00000496328.2:n.*361+10_*361+14delins...
ENST00000646926.2:c.*39+10_*39+14delinsTTCTC	ENSP00000494215.2:n.*39+10_*39+14delinsTT...
ENST00000682004.1:n.2469+10_2469+14delinsTTCTC
ENST00000682299.1:c.1002+1306_1002+1310delinsTTCTC	ENSP00000506811.1:n.1002+1306_1002+1310de...
ENST00000682392.1:c.1079+10_1079+14delinsTTCTC	ENSP00000508314.1:n.1079+10_1079+14delins...
ENST00000682641.1:c.1079+10_1079+14delinsTTCTC	ENSP00000506793.1:n.1079+10_1079+14delins...
ENST00000683439.1:n.3362+10_3362+14delinsTTCTC
ENST00000683724.1:c.1079+10_1079+14delinsTTCTC	ENSP00000507984.1:n.1079+10_1079+14delins...
ENST00000684301.1:c.*478+10_*478+14delinsTTCTC	ENSP00000507824.1:n.*478+10_*478+14delins...
ENST00000684605.1:n.1619+10_1619+14delinsTTCTC
ENST00000684658.1:n.1224+10_1224+14delinsTTCTC
ENST00000684715.1:n.1224+10_1224+14delinsTTCTC
ENST00000684765.1:c.1079+10_1079+14delinsTTCTC	ENSP00000507910.1:n.1079+10_1079+14delins...
ENST00000336451.8:c.*478+10_*478+14delinsTTCTC	ENSP00000336683.4:n.*478+10_*478+14delins...
ENST00000444024.3:c.1079+10_1079+14delinsTTCTC MANE Select	ENSP00000412708.2:n.1079+10_1079+14delins...
ENST00000622845.5:c.569+10_569+14delinsTTCTC	ENSP00000481280.1:n.569+10_569+14delinsTT...
ENST00000644054.1:c.1002+10_1002+14delinsTTCTC
ENST00000644711.1:c.1079+10_1079+14delinsTTCTC	ENSP00000494106.1:n.1079+10_1079+14delins...
ENST00000645367.1:n.1067_1071delinsTTCTC
ENST00000645895.1:n.1196+10_1196+14delinsTTCTC
ENST00000646926.1:c.422+10_422+14delinsTTCTC
ENST00000336451.7:c.446+10_446+14delinsTTCTC	ENSP00000336683.3:n.446+10_446+14delinsTT...
ENST00000367303.8:c.1079+10_1079+14delinsTTCTC	ENSP00000356272.4:n.1079+10_1079+14delins...
ENST00000444024.1:c.569+10_569+14delinsTTCTC	ENSP00000412708.1:n.569+10_569+14delinsTT...
ENST00000622845.4:c.569+10_569+14delinsTTCTC	ENSP00000481280.1:n.569+10_569+14delinsTT...
NM_001271937.1:c.569+10_569+14delinsTTCTC	NP_001258866.1:n.569+10_569+14delinsTTCTC...
NM_017909.3:c.1079+10_1079+14delinsTTCTC	NP_060379.2:n.1079+10_1079+14delinsTTCTC
XM_005267040.2:c.446+10_446+14delinsTTCTC	XP_005267097.1:n.446+10_446+14delinsTTCTC...
XR_942497.1:n.1259+10_1259+14delinsTTCTC
XM_005267040.4:c.446+10_446+14delinsTTCTC	XP_005267097.1:n.446+10_446+14delinsTTCTC...
XM_017010988.2:c.446+10_446+14delinsTTCTC	XP_016866477.1:n.446+10_446+14delinsTTCTC...
XR_001743503.2:n.1247+10_1247+14delinsTTCTC
XR_002956288.1:n.1204+10_1204+14delinsTTCTC
NM_017909.4:c.1079+10_1079+14delinsTTCTC MANE Select	NP_060379.2:n.1079+10_1079+14delinsTTCTC
NM_001271937.2:c.569+10_569+14delinsTTCTC	NP_001258866.1:n.569+10_569+14delinsTTCTC...