Canonical Allele Identifier: CA366059224

Gene: RMND1

Linked Data

• MyVariant Identifiers: chr6:g.151742380C>G (hg19) ; chr6:g.151421245C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421245C>G , CM000668.2:g.151421245C>G	GRCh38
NC_000006.11:g.151742380C>G , CM000668.1:g.151742380C>G	GRCh37
NC_000006.10:g.151784073C>G	NCBI36
NG_033031.1:g.35937G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644054.2:c.*361G>C	ENSP00000496328.2:n.*361G>C
ENST00000646926.2:c.*39G>C	ENSP00000494215.2:n.*39G>C
ENST00000682004.1:n.2469G>C
ENST00000682299.1:c.1002+1296G>C	ENSP00000506811.1:n.1002+1296G>C
ENST00000682392.1:c.1079G>C	ENSP00000508314.1:p.Arg360Thr
ENST00000682641.1:c.1079G>C	ENSP00000506793.1:p.Arg360Thr
ENST00000683439.1:n.3362G>C
ENST00000683724.1:c.1079G>C	ENSP00000507984.1:p.Arg360Thr
ENST00000684301.1:c.*478G>C	ENSP00000507824.1:n.*478G>C
ENST00000684605.1:n.1619G>C
ENST00000684658.1:n.1224G>C
ENST00000684715.1:n.1224G>C
ENST00000684765.1:c.1079G>C	ENSP00000507910.1:p.Arg360Thr
ENST00000336451.8:c.*478G>C	ENSP00000336683.4:n.*478G>C
ENST00000444024.3:c.1079G>C MANE Select	ENSP00000412708.2:p.Arg360Thr
ENST00000622845.5:c.569G>C	ENSP00000481280.1:p.Arg190Thr
ENST00000644054.1:c.1002G>C
ENST00000644711.1:c.1079G>C	ENSP00000494106.1:p.Arg360Thr
ENST00000645367.1:n.1057G>C
ENST00000645895.1:n.1196G>C
ENST00000646926.1:c.422G>C
ENST00000336451.7:c.446G>C	ENSP00000336683.3:p.Arg149Thr
ENST00000367303.8:c.1079G>C	ENSP00000356272.4:p.Arg360Thr
ENST00000444024.1:c.569G>C	ENSP00000412708.1:p.Arg190Thr
ENST00000622845.4:c.569G>C	ENSP00000481280.1:p.Arg190Thr
NM_001271937.1:c.569G>C	NP_001258866.1:p.Arg190Thr
NM_017909.3:c.1079G>C	NP_060379.2:p.Arg360Thr
XM_005267040.2:c.446G>C	XP_005267097.1:p.Arg149Thr
XR_942497.1:n.1259G>C
XM_005267040.4:c.446G>C	XP_005267097.1:p.Arg149Thr
XM_017010988.2:c.446G>C	XP_016866477.1:p.Arg149Thr
XR_001743503.2:n.1247G>C
XR_002956288.1:n.1204G>C
NM_017909.4:c.1079G>C MANE Select	NP_060379.2:p.Arg360Thr
NM_001271937.2:c.569G>C	NP_001258866.1:p.Arg190Thr