Canonical Allele Identifier: CA150120222
Community Standard Title: NM_017909.4(RMND1):c.613+333dup
Gene: RMND1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151436126dup , CM000668.2:g.151436126dup GRCh38
NC_000006.11:g.151757261dup , CM000668.1:g.151757261dup GRCh37
NC_000006.10:g.151798954dup NCBI36
NG_033031.1:g.21069dup

Transcript Alleles

HGVS Amino-acid Change
NM_017909.4:c.613+333dup MANE Select NP_060379.2:n.613+333dup
ENST00000444024.3:c.613+333dup MANE Select ENSP00000412708.2:n.613+333dup
NM_001271937.1:c.103+333dup NP_001258866.1:n.103+333dup
NM_001271937.2:c.103+333dup NP_001258866.1:n.103+333dup
NM_017909.3:c.613+333dup NP_060379.2:n.613+333dup
ENST00000336451.7:c.-21+307dup ENSP00000336683.3:n.-21+307dup
ENST00000336451.8:c.*12+307dup ENSP00000336683.4:n.*12+307dup
ENST00000367303.8:c.613+333dup ENSP00000356272.4:n.613+333dup
ENST00000444024.1:c.103+333dup ENSP00000412708.1:n.103+333dup
ENST00000622845.4:c.103+333dup ENSP00000481280.1:n.103+333dup
ENST00000622845.5:c.103+333dup ENSP00000481280.1:n.103+333dup
ENST00000643550.1:n.407+307dup
ENST00000644054.1:c.510+333dup
ENST00000644054.2:c.613+333dup ENSP00000496328.2:n.613+333dup
ENST00000644711.1:c.613+333dup ENSP00000494106.1:n.613+333dup
ENST00000645367.1:n.757+333dup
ENST00000645895.1:n.730+307dup
ENST00000646926.1:c.21+333dup
ENST00000646926.2:c.613+333dup ENSP00000494215.2:n.613+333dup
ENST00000682004.1:n.784+307dup
ENST00000682299.1:c.613+333dup ENSP00000506811.1:n.613+333dup
ENST00000682392.1:c.613+333dup ENSP00000508314.1:n.613+333dup
ENST00000682641.1:c.613+333dup ENSP00000506793.1:n.613+333dup
ENST00000682760.1:n.758+333dup
ENST00000683439.1:n.758+333dup
ENST00000683724.1:c.613+333dup ENSP00000507984.1:n.613+333dup
ENST00000683740.1:n.758+333dup
ENST00000684301.1:c.*12+307dup ENSP00000507824.1:n.*12+307dup
ENST00000684658.1:n.758+333dup
ENST00000684715.1:n.758+333dup
ENST00000684765.1:c.613+333dup ENSP00000507910.1:n.613+333dup
XM_005267040.2:c.-21+307dup XP_005267097.1:n.-21+307dup
XM_005267040.4:c.-21+307dup XP_005267097.1:n.-21+307dup
XM_017010988.2:c.-21+307dup XP_016866477.1:n.-21+307dup
XR_001743503.2:n.781+333dup
XR_002956288.1:n.738+333dup
XR_942497.1:n.793+333dup