Canonical Allele Identifier: CA2680794026

Gene: RMND1

Linked Data

• gnomAD v4: 6-151430199-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151430199A>G , CM000668.2:g.151430199A>G	GRCh38
NC_000006.11:g.151751334A>G , CM000668.1:g.151751334A>G	GRCh37
NC_000006.10:g.151793027A>G	NCBI36
NG_033031.1:g.26983T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644054.2:c.694T>C	ENSP00000496328.2:p.Phe232Leu
ENST00000646926.2:c.690-22T>C	ENSP00000494215.2:n.690-22T>C
ENST00000682004.1:n.861-22T>C
ENST00000682299.1:c.690-22T>C	ENSP00000506811.1:n.690-22T>C
ENST00000682392.1:c.690-22T>C	ENSP00000508314.1:n.690-22T>C
ENST00000682641.1:c.690-22T>C	ENSP00000506793.1:n.690-22T>C
ENST00000682760.1:n.835-22T>C
ENST00000683439.1:n.835-22T>C
ENST00000683724.1:c.690-22T>C	ENSP00000507984.1:n.690-22T>C
ENST00000683740.1:n.835-22T>C
ENST00000684301.1:c.*89-22T>C	ENSP00000507824.1:n.*89-22T>C
ENST00000684605.1:n.1230-22T>C
ENST00000684658.1:n.835-22T>C
ENST00000684715.1:n.835-22T>C
ENST00000684765.1:c.690-22T>C	ENSP00000507910.1:n.690-22T>C
ENST00000336451.8:c.*89-22T>C	ENSP00000336683.4:n.*89-22T>C
ENST00000444024.3:c.690-22T>C MANE Select	ENSP00000412708.2:n.690-22T>C
ENST00000622845.5:c.180-22T>C	ENSP00000481280.1:n.180-22T>C
ENST00000643550.1:n.484-22T>C
ENST00000644054.1:c.591T>C
ENST00000644711.1:c.690-22T>C	ENSP00000494106.1:n.690-22T>C
ENST00000645367.1:n.834-22T>C
ENST00000645895.1:n.807-22T>C
ENST00000646926.1:c.98-22T>C
ENST00000336451.7:c.57-22T>C	ENSP00000336683.3:n.57-22T>C
ENST00000367303.8:c.690-22T>C	ENSP00000356272.4:n.690-22T>C
ENST00000444024.1:c.180-22T>C	ENSP00000412708.1:n.180-22T>C
ENST00000622845.4:c.180-22T>C	ENSP00000481280.1:n.180-22T>C
NM_001271937.1:c.180-22T>C	NP_001258866.1:n.180-22T>C
NM_017909.3:c.690-22T>C	NP_060379.2:n.690-22T>C
XM_005267040.2:c.57-22T>C	XP_005267097.1:n.57-22T>C
XR_942497.1:n.870-22T>C
XM_005267040.4:c.57-22T>C	XP_005267097.1:n.57-22T>C
XM_017010988.2:c.57-22T>C	XP_016866477.1:n.57-22T>C
XR_001743503.2:n.858-22T>C
XR_002956288.1:n.815-22T>C
NM_017909.4:c.690-22T>C MANE Select	NP_060379.2:n.690-22T>C
NM_001271937.2:c.180-22T>C	NP_001258866.1:n.180-22T>C