Canonical Allele Identifier: CA366057779

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151417381A>T , CM000668.2:g.151417381A>T	GRCh38
NC_000006.11:g.151738516A>T , CM000668.1:g.151738516A>T	GRCh37
NC_000006.10:g.151780209A>T	NCBI36
NG_033031.1:g.39801T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644054.2:c.*380T>A	ENSP00000496328.2:n.*380T>A
ENST00000646926.2:c.*58T>A	ENSP00000494215.2:n.*58T>A
ENST00000682004.1:n.2488T>A
ENST00000682299.1:c.1002+5160T>A	ENSP00000506811.1:n.1002+5160T>A
ENST00000682392.1:c.1098T>A	ENSP00000508314.1:p.Ser366Arg
ENST00000682641.1:c.1098T>A	ENSP00000506793.1:p.Ser366Arg
ENST00000683439.1:n.3381T>A
ENST00000683724.1:c.1098T>A	ENSP00000507984.1:p.Ser366Arg
ENST00000684301.1:c.*497T>A	ENSP00000507824.1:n.*497T>A
ENST00000684605.1:n.1638T>A
ENST00000684658.1:n.1243T>A
ENST00000684715.1:n.1243T>A
ENST00000684765.1:c.*26T>A	ENSP00000507910.1:n.*26T>A
ENST00000336451.8:c.*497T>A	ENSP00000336683.4:n.*497T>A
ENST00000444024.3:c.1098T>A MANE Select	ENSP00000412708.2:p.Ser366Arg
ENST00000622845.5:c.588T>A	ENSP00000481280.1:p.Ser196Arg
ENST00000644054.1:c.1021T>A
ENST00000644711.1:c.1098T>A	ENSP00000494106.1:p.Ser366Arg
ENST00000645895.1:n.1262T>A
ENST00000646926.1:c.441T>A
ENST00000336451.7:c.465T>A	ENSP00000336683.3:p.Ser155Arg
ENST00000367303.8:c.1098T>A	ENSP00000356272.4:p.Ser366Arg
ENST00000444024.1:c.588T>A	ENSP00000412708.1:p.Ser196Arg
ENST00000622845.4:c.588T>A	ENSP00000481280.1:p.Ser196Arg
NM_001271937.1:c.588T>A	NP_001258866.1:p.Ser196Arg
NM_017909.3:c.1098T>A	NP_060379.2:p.Ser366Arg
XM_005267040.2:c.465T>A	XP_005267097.1:p.Ser155Arg
XR_942497.1:n.1278T>A
XM_005267040.4:c.465T>A	XP_005267097.1:p.Ser155Arg
XM_017010988.2:c.465T>A	XP_016866477.1:p.Ser155Arg
XR_001743503.2:n.1266T>A
XR_002956288.1:n.1223T>A
NM_017909.4:c.1098T>A MANE Select	NP_060379.2:p.Ser366Arg
NM_001271937.2:c.588T>A	NP_001258866.1:p.Ser196Arg