Canonical Allele Identifier: CA366059229

Gene: RMND1

Linked Data

• MyVariant Identifiers: chr6:g.151742381T>A (hg19) ; chr6:g.151421246T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421246T>A , CM000668.2:g.151421246T>A	GRCh38
NC_000006.11:g.151742381T>A , CM000668.1:g.151742381T>A	GRCh37
NC_000006.10:g.151784074T>A	NCBI36
NG_033031.1:g.35936A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644054.2:c.*360A>T	ENSP00000496328.2:n.*360A>T
ENST00000646926.2:c.*38A>T	ENSP00000494215.2:n.*38A>T
ENST00000682004.1:n.2468A>T
ENST00000682299.1:c.1002+1295A>T	ENSP00000506811.1:n.1002+1295A>T
ENST00000682392.1:c.1078A>T	ENSP00000508314.1:p.Arg360Trp
ENST00000682641.1:c.1078A>T	ENSP00000506793.1:p.Arg360Trp
ENST00000683439.1:n.3361A>T
ENST00000683724.1:c.1078A>T	ENSP00000507984.1:p.Arg360Trp
ENST00000684301.1:c.*477A>T	ENSP00000507824.1:n.*477A>T
ENST00000684605.1:n.1618A>T
ENST00000684658.1:n.1223A>T
ENST00000684715.1:n.1223A>T
ENST00000684765.1:c.1078A>T	ENSP00000507910.1:p.Arg360Trp
ENST00000336451.8:c.*477A>T	ENSP00000336683.4:n.*477A>T
ENST00000444024.3:c.1078A>T MANE Select	ENSP00000412708.2:p.Arg360Trp
ENST00000622845.5:c.568A>T	ENSP00000481280.1:p.Arg190Trp
ENST00000644054.1:c.1001A>T
ENST00000644711.1:c.1078A>T	ENSP00000494106.1:p.Arg360Trp
ENST00000645367.1:n.1056A>T
ENST00000645895.1:n.1195A>T
ENST00000646926.1:c.421A>T
ENST00000336451.7:c.445A>T	ENSP00000336683.3:p.Arg149Trp
ENST00000367303.8:c.1078A>T	ENSP00000356272.4:p.Arg360Trp
ENST00000444024.1:c.568A>T	ENSP00000412708.1:p.Arg190Trp
ENST00000622845.4:c.568A>T	ENSP00000481280.1:p.Arg190Trp
NM_001271937.1:c.568A>T	NP_001258866.1:p.Arg190Trp
NM_017909.3:c.1078A>T	NP_060379.2:p.Arg360Trp
XM_005267040.2:c.445A>T	XP_005267097.1:p.Arg149Trp
XR_942497.1:n.1258A>T
XM_005267040.4:c.445A>T	XP_005267097.1:p.Arg149Trp
XM_017010988.2:c.445A>T	XP_016866477.1:p.Arg149Trp
XR_001743503.2:n.1246A>T
XR_002956288.1:n.1203A>T
NM_017909.4:c.1078A>T MANE Select	NP_060379.2:p.Arg360Trp
NM_001271937.2:c.568A>T	NP_001258866.1:p.Arg190Trp