Canonical Allele Identifier: CA4051067

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151445522del , CM000668.2:g.151445522del	GRCh38
NC_000006.11:g.151766657del , CM000668.1:g.151766657del	GRCh37
NC_000006.10:g.151808350del	NCBI36
NG_033031.1:g.11661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644054.2:c.291del	ENSP00000496328.2:p.Met98Ter
ENST00000646926.2:c.291del	ENSP00000494215.2:p.Met98Ter
ENST00000682004.1:n.436del
ENST00000682299.1:c.291del	ENSP00000506811.1:p.Met98Ter
ENST00000682392.1:c.291del	ENSP00000508314.1:p.Met98Ter
ENST00000682641.1:c.291del	ENSP00000506793.1:p.Met98Ter
ENST00000682760.1:n.436del
ENST00000683439.1:n.436del
ENST00000683724.1:c.291del	ENSP00000507984.1:p.Met98Ter
ENST00000683740.1:n.436del
ENST00000684301.1:c.291del	ENSP00000507824.1:p.Met98Ter
ENST00000684658.1:n.436del
ENST00000684715.1:n.436del
ENST00000684765.1:c.291del	ENSP00000507910.1:p.Met98Ter
ENST00000444024.3:c.291del MANE Select	ENSP00000412708.2:p.Met98Ter
ENST00000491268.2:c.291del	ENSP00000494948.1:p.Met98Ter
ENST00000622845.5:c.-7+6495del	ENSP00000481280.1:n.-7+6495del
ENST00000643564.1:n.364del
ENST00000644054.1:c.188del
ENST00000644711.1:c.291del	ENSP00000494106.1:p.Met98Ter
ENST00000645367.1:n.435del
ENST00000645895.1:n.382del
ENST00000645917.1:n.510del
ENST00000367303.8:c.291del	ENSP00000356272.4:p.Met98Ter
ENST00000444024.1:c.-7+6495del	ENSP00000412708.1:n.-7+6495del
ENST00000491268.1:n.305del
ENST00000622845.4:c.-7+6495del	ENSP00000481280.1:n.-7+6495del
NM_001271937.1:c.-7+6495del	NP_001258866.1:n.-7+6495del
NM_017909.3:c.291del	NP_060379.2:p.Met98Ter
XR_942497.1:n.471del
XM_005267040.4:c.-156+6495del	XP_005267097.1:n.-156+6495del
XM_017010988.2:c.-369del	XP_016866477.1:n.-369del
XR_001743503.2:n.459del
XR_002956288.1:n.416del
NM_017909.4:c.291del MANE Select	NP_060379.2:p.Met98Ter
NM_001271937.2:c.-7+6495del	NP_001258866.1:n.-7+6495del