Canonical Allele Identifier: CA2578772080
Gene: RMND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151421250_151421251del , CM000668.2:g.151421250_151421251del GRCh38
NC_000006.11:g.151742385_151742386del , CM000668.1:g.151742385_151742386del GRCh37
NC_000006.10:g.151784078_151784079del NCBI36
NG_033031.1:g.35933_35934del

Transcript Alleles

HGVS Amino-acid change
ENST00000644054.2:c.*357_*358del ENSP00000496328.2:n.*357_*358del
ENST00000646926.2:c.*35_*36del ENSP00000494215.2:n.*35_*36del
ENST00000682004.1:n.2465_2466del
ENST00000682299.1:c.1002+1292_1002+1293del ENSP00000506811.1:n.1002+1292_1002+1293de...
ENST00000682392.1:c.1075_1076del ENSP00000508314.1:p.Leu359LysfsTer15
ENST00000682641.1:c.1075_1076del ENSP00000506793.1:p.Leu359LysfsTer15
ENST00000683439.1:n.3358_3359del
ENST00000683724.1:c.1075_1076del ENSP00000507984.1:p.Leu359LysfsTer15
ENST00000684301.1:c.*474_*475del ENSP00000507824.1:n.*474_*475del
ENST00000684605.1:n.1615_1616del
ENST00000684658.1:n.1220_1221del
ENST00000684715.1:n.1220_1221del
ENST00000684765.1:c.1075_1076del ENSP00000507910.1:p.Leu359LysfsTer?
ENST00000336451.8:c.*474_*475del ENSP00000336683.4:n.*474_*475del
ENST00000444024.3:c.1075_1076del MANE Select ENSP00000412708.2:p.Leu359LysfsTer15
ENST00000622845.5:c.565_566del ENSP00000481280.1:p.Leu189LysfsTer15
ENST00000644054.1:c.998_999del
ENST00000644711.1:c.1075_1076del ENSP00000494106.1:p.Leu359LysfsTer15
ENST00000645367.1:n.1053_1054del
ENST00000645895.1:n.1192_1193del
ENST00000646926.1:c.418_419del
ENST00000336451.7:c.442_443del ENSP00000336683.3:p.Leu148LysfsTer15
ENST00000367303.8:c.1075_1076del ENSP00000356272.4:p.Leu359LysfsTer15
ENST00000444024.1:c.565_566del ENSP00000412708.1:p.Leu189LysfsTer15
ENST00000622845.4:c.565_566del ENSP00000481280.1:p.Leu189LysfsTer15
NM_001271937.1:c.565_566del NP_001258866.1:p.Leu189LysfsTer15
NM_017909.3:c.1075_1076del NP_060379.2:p.Leu359LysfsTer15
XM_005267040.2:c.442_443del XP_005267097.1:p.Leu148LysfsTer15
XR_942497.1:n.1255_1256del
XM_005267040.4:c.442_443del XP_005267097.1:p.Leu148LysfsTer15
XM_017010988.2:c.442_443del XP_016866477.1:p.Leu148LysfsTer15
XR_001743503.2:n.1243_1244del
XR_002956288.1:n.1200_1201del
NM_017909.4:c.1075_1076del MANE Select NP_060379.2:p.Leu359LysfsTer15
NM_001271937.2:c.565_566del NP_001258866.1:p.Leu189LysfsTer15