Canonical Allele Identifier: CA150093875

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151406119T>C , CM000668.2:g.151406119T>C	GRCh38
NC_000006.11:g.151727254T>C , CM000668.1:g.151727254T>C	GRCh37
NC_000006.10:g.151768947T>C	NCBI36
NG_033031.1:g.51063A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644054.2:c.*483-283A>G	ENSP00000496328.2:n.*483-283A>G
ENST00000646926.2:c.*161-283A>G	ENSP00000494215.2:n.*161-283A>G
ENST00000682004.1:n.2591-283A>G
ENST00000682299.1:c.1003-283A>G	ENSP00000506811.1:n.1003-283A>G
ENST00000682392.1:c.*2-283A>G	ENSP00000508314.1:n.*2-283A>G
ENST00000682641.1:c.1201-283A>G	ENSP00000506793.1:n.1201-283A>G
ENST00000683439.1:n.3484-283A>G
ENST00000683724.1:c.1201-283A>G	ENSP00000507984.1:n.1201-283A>G
ENST00000684301.1:c.*673-283A>G	ENSP00000507824.1:n.*673-283A>G
ENST00000684605.1:n.1741-283A>G
ENST00000684765.1:c.*129-283A>G	ENSP00000507910.1:n.*129-283A>G
ENST00000336451.8:c.*600-283A>G	ENSP00000336683.4:n.*600-283A>G
ENST00000444024.3:c.1201-283A>G MANE Select	ENSP00000412708.2:n.1201-283A>G
ENST00000622845.5:c.691-283A>G	ENSP00000481280.1:n.691-283A>G
ENST00000644054.1:c.1124-283A>G
ENST00000644711.1:c.*124-283A>G	ENSP00000494106.1:n.*124-283A>G
ENST00000646926.1:c.544-283A>G
ENST00000336451.7:c.568-283A>G	ENSP00000336683.3:n.568-283A>G
ENST00000367303.8:c.1201-283A>G	ENSP00000356272.4:n.1201-283A>G
ENST00000622845.4:c.691-283A>G	ENSP00000481280.1:n.691-283A>G
NM_001271937.1:c.691-283A>G	NP_001258866.1:n.691-283A>G
NM_017909.3:c.1201-283A>G	NP_060379.2:n.1201-283A>G
XM_005267040.2:c.568-283A>G	XP_005267097.1:n.568-283A>G
XR_942497.1:n.1639-283A>G
XM_005267040.4:c.568-283A>G	XP_005267097.1:n.568-283A>G
XM_017010988.2:c.568-283A>G	XP_016866477.1:n.568-283A>G
XR_001743503.2:n.1369-283A>G
XR_002956288.1:n.1584-283A>G
NM_017909.4:c.1201-283A>G MANE Select	NP_060379.2:n.1201-283A>G
NM_001271937.2:c.691-283A>G	NP_001258866.1:n.691-283A>G