Canonical Allele Identifier: CA1672873156

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421191_151421208delinsTTTCTTGAGATTGTTAAA , CM000668.2:g.151421191_151421208delinsTTTCTTGAGATTGTTAAA	GRCh38
NC_000006.11:g.151742326_151742343delinsTTTCTTGAGATTGTTAAA , CM000668.1:g.151742326_151742343delinsTTTCTTGAGATTGTTAAA	GRCh37
NC_000006.10:g.151784019_151784036delinsTTTCTTGAGATTGTTAAA	NCBI36
NG_033031.1:g.35974_35991delinsTTTAACAATCTCAAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644054.2:c.*361+37_*361+54delinsTTTAACAATCTCAAGAAA	ENSP00000496328.2:n.*361+37_*361+54delinsTTTAACAATCTCAAGAAA
ENST00000646926.2:c.*39+37_*39+54delinsTTTAACAATCTCAAGAAA	ENSP00000494215.2:n.*39+37_*39+54delinsTTTAACAATCTCAAGAAA
ENST00000682004.1:n.2469+37_2469+54delinsTTTAACAATCTCAAGAAA
ENST00000682299.1:c.1002+1333_1002+1350delinsTTTAACAATCTCAAGAAA	ENSP00000506811.1:n.1002+1333_1002+1350delinsTTTAACAATCTCAAGA...
ENST00000682392.1:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA	ENSP00000508314.1:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
ENST00000682641.1:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA	ENSP00000506793.1:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
ENST00000683439.1:n.3362+37_3362+54delinsTTTAACAATCTCAAGAAA
ENST00000683724.1:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA	ENSP00000507984.1:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
ENST00000684301.1:c.*478+37_*478+54delinsTTTAACAATCTCAAGAAA	ENSP00000507824.1:n.*478+37_*478+54delinsTTTAACAATCTCAAGAAA
ENST00000684605.1:n.1619+37_1619+54delinsTTTAACAATCTCAAGAAA
ENST00000684658.1:n.1224+37_1224+54delinsTTTAACAATCTCAAGAAA
ENST00000684715.1:n.1224+37_1224+54delinsTTTAACAATCTCAAGAAA
ENST00000684765.1:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA	ENSP00000507910.1:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
ENST00000336451.8:c.*478+37_*478+54delinsTTTAACAATCTCAAGAAA	ENSP00000336683.4:n.*478+37_*478+54delinsTTTAACAATCTCAAGAAA
ENST00000444024.3:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA MANE Select	ENSP00000412708.2:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
ENST00000622845.5:c.569+37_569+54delinsTTTAACAATCTCAAGAAA	ENSP00000481280.1:n.569+37_569+54delinsTTTAACAATCTCAAGAAA
ENST00000644054.1:c.1002+37_1002+54delinsTTTAACAATCTCAAGAAA
ENST00000644711.1:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA	ENSP00000494106.1:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
ENST00000645367.1:n.1094_1111delinsTTTAACAATCTCAAGAAA
ENST00000645895.1:n.1196+37_1196+54delinsTTTAACAATCTCAAGAAA
ENST00000646926.1:c.422+37_422+54delinsTTTAACAATCTCAAGAAA
ENST00000336451.7:c.446+37_446+54delinsTTTAACAATCTCAAGAAA	ENSP00000336683.3:n.446+37_446+54delinsTTTAACAATCTCAAGAAA
ENST00000367303.8:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA	ENSP00000356272.4:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
ENST00000444024.1:c.569+37_569+54delinsTTTAACAATCTCAAGAAA	ENSP00000412708.1:n.569+37_569+54delinsTTTAACAATCTCAAGAAA
ENST00000622845.4:c.569+37_569+54delinsTTTAACAATCTCAAGAAA	ENSP00000481280.1:n.569+37_569+54delinsTTTAACAATCTCAAGAAA
NM_001271937.1:c.569+37_569+54delinsTTTAACAATCTCAAGAAA	NP_001258866.1:n.569+37_569+54delinsTTTAACAATCTCAAGAAA
NM_017909.3:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA	NP_060379.2:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
XM_005267040.2:c.446+37_446+54delinsTTTAACAATCTCAAGAAA	XP_005267097.1:n.446+37_446+54delinsTTTAACAATCTCAAGAAA
XR_942497.1:n.1259+37_1259+54delinsTTTAACAATCTCAAGAAA
XM_005267040.4:c.446+37_446+54delinsTTTAACAATCTCAAGAAA	XP_005267097.1:n.446+37_446+54delinsTTTAACAATCTCAAGAAA
XM_017010988.2:c.446+37_446+54delinsTTTAACAATCTCAAGAAA	XP_016866477.1:n.446+37_446+54delinsTTTAACAATCTCAAGAAA
XR_001743503.2:n.1247+37_1247+54delinsTTTAACAATCTCAAGAAA
XR_002956288.1:n.1204+37_1204+54delinsTTTAACAATCTCAAGAAA
NM_017909.4:c.1079+37_1079+54delinsTTTAACAATCTCAAGAAA MANE Select	NP_060379.2:n.1079+37_1079+54delinsTTTAACAATCTCAAGAAA
NM_001271937.2:c.569+37_569+54delinsTTTAACAATCTCAAGAAA	NP_001258866.1:n.569+37_569+54delinsTTTAACAATCTCAAGAAA