Canonical Allele Identifier: CA366059196

Gene: RMND1

Linked Data

• MyVariant Identifiers: chr6:g.151742378A>C (hg19) ; chr6:g.151421243A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421243A>C , CM000668.2:g.151421243A>C	GRCh38
NC_000006.11:g.151742378A>C , CM000668.1:g.151742378A>C	GRCh37
NC_000006.10:g.151784071A>C	NCBI36
NG_033031.1:g.35939T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644054.2:c.*361+2T>G	ENSP00000496328.2:n.*361+2T>G
ENST00000646926.2:c.*39+2T>G	ENSP00000494215.2:n.*39+2T>G
ENST00000682004.1:n.2469+2T>G
ENST00000682299.1:c.1002+1298T>G	ENSP00000506811.1:n.1002+1298T>G
ENST00000682392.1:c.1079+2T>G	ENSP00000508314.1:n.1079+2T>G
ENST00000682641.1:c.1079+2T>G	ENSP00000506793.1:n.1079+2T>G
ENST00000683439.1:n.3362+2T>G
ENST00000683724.1:c.1079+2T>G	ENSP00000507984.1:n.1079+2T>G
ENST00000684301.1:c.*478+2T>G	ENSP00000507824.1:n.*478+2T>G
ENST00000684605.1:n.1619+2T>G
ENST00000684658.1:n.1224+2T>G
ENST00000684715.1:n.1224+2T>G
ENST00000684765.1:c.1079+2T>G	ENSP00000507910.1:n.1079+2T>G
ENST00000336451.8:c.*478+2T>G	ENSP00000336683.4:n.*478+2T>G
ENST00000444024.3:c.1079+2T>G MANE Select	ENSP00000412708.2:n.1079+2T>G
ENST00000622845.5:c.569+2T>G	ENSP00000481280.1:n.569+2T>G
ENST00000644054.1:c.1002+2T>G
ENST00000644711.1:c.1079+2T>G	ENSP00000494106.1:n.1079+2T>G
ENST00000645367.1:n.1059T>G
ENST00000645895.1:n.1196+2T>G
ENST00000646926.1:c.422+2T>G
ENST00000336451.7:c.446+2T>G	ENSP00000336683.3:n.446+2T>G
ENST00000367303.8:c.1079+2T>G	ENSP00000356272.4:n.1079+2T>G
ENST00000444024.1:c.569+2T>G	ENSP00000412708.1:n.569+2T>G
ENST00000622845.4:c.569+2T>G	ENSP00000481280.1:n.569+2T>G
NM_001271937.1:c.569+2T>G	NP_001258866.1:n.569+2T>G
NM_017909.3:c.1079+2T>G	NP_060379.2:n.1079+2T>G
XM_005267040.2:c.446+2T>G	XP_005267097.1:n.446+2T>G
XR_942497.1:n.1259+2T>G
XM_005267040.4:c.446+2T>G	XP_005267097.1:n.446+2T>G
XM_017010988.2:c.446+2T>G	XP_016866477.1:n.446+2T>G
XR_001743503.2:n.1247+2T>G
XR_002956288.1:n.1204+2T>G
NM_017909.4:c.1079+2T>G MANE Select	NP_060379.2:n.1079+2T>G
NM_001271937.2:c.569+2T>G	NP_001258866.1:n.569+2T>G