Canonical Allele Identifier: CA12253340

Gene: RMND1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151405040G>T , CM000668.2:g.151405040G>T	GRCh38
NC_000006.11:g.151726175G>T , CM000668.1:g.151726175G>T	GRCh37
NC_000006.10:g.151767868G>T	NCBI36
NG_033031.1:g.52142C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_017909.4:c.*195C>A MANE Select	NP_060379.2:n.*195C>A
ENST00000444024.3:c.*195C>A MANE Select	ENSP00000412708.2:n.*195C>A
NM_001271937.1:c.*195C>A	NP_001258866.1:n.*195C>A
NM_001271937.2:c.*195C>A	NP_001258866.1:n.*195C>A
NM_017909.3:c.*195C>A	NP_060379.2:n.*195C>A
ENST00000336451.7:c.*195C>A	ENSP00000336683.3:n.*195C>A
ENST00000336451.8:c.*944C>A	ENSP00000336683.4:n.*944C>A
ENST00000367303.8:c.*195C>A	ENSP00000356272.4:n.*195C>A
ENST00000622845.4:c.*195C>A	ENSP00000481280.1:n.*195C>A
ENST00000622845.5:c.*195C>A	ENSP00000481280.1:n.*195C>A
ENST00000646926.1:c.888C>A
ENST00000646926.2:c.*505C>A	ENSP00000494215.2:n.*505C>A
ENST00000682004.1:n.2935C>A
ENST00000682299.1:c.*195C>A	ENSP00000506811.1:n.*195C>A
ENST00000682392.1:c.*346C>A	ENSP00000508314.1:n.*346C>A
ENST00000682641.1:c.1317+680C>A	ENSP00000506793.1:n.1317+680C>A
ENST00000683439.1:n.3828C>A
ENST00000683724.1:c.*195C>A	ENSP00000507984.1:n.*195C>A
ENST00000684605.1:n.2085C>A
ENST00000684765.1:c.*473C>A	ENSP00000507910.1:n.*473C>A
XM_005267040.2:c.*195C>A	XP_005267097.1:n.*195C>A
XM_005267040.4:c.*195C>A	XP_005267097.1:n.*195C>A
XM_017010988.2:c.*195C>A	XP_016866477.1:n.*195C>A
XR_001743503.2:n.1713C>A
XR_002956288.1:n.1928C>A