Canonical Allele Identifier: CA820802395

Gene: RMND1

Linked Data

• dbSNP Id: rs1324482534
• gnomAD v3: 6-151421227-TAG-T
• gnomAD v4: 6-151421227-TAG-T
• MyVariant Identifiers: chr6:g.151742363_151742364del (hg19) ; chr6:g.151421228_151421229del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151421233_151421234del , CM000668.2:g.151421233_151421234del	GRCh38
NC_000006.11:g.151742368_151742369del , CM000668.1:g.151742368_151742369del	GRCh37
NC_000006.10:g.151784061_151784062del	NCBI36
NG_033031.1:g.35953_35954del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644054.2:c.*361+16_*361+17del	ENSP00000496328.2:n.*361+16_*361+17del
ENST00000646926.2:c.*39+16_*39+17del	ENSP00000494215.2:n.*39+16_*39+17del
ENST00000682004.1:n.2469+16_2469+17del
ENST00000682299.1:c.1002+1312_1002+1313del	ENSP00000506811.1:n.1002+1312_1002+1313de...
ENST00000682392.1:c.1079+16_1079+17del	ENSP00000508314.1:n.1079+16_1079+17del
ENST00000682641.1:c.1079+16_1079+17del	ENSP00000506793.1:n.1079+16_1079+17del
ENST00000683439.1:n.3362+16_3362+17del
ENST00000683724.1:c.1079+16_1079+17del	ENSP00000507984.1:n.1079+16_1079+17del
ENST00000684301.1:c.*478+16_*478+17del	ENSP00000507824.1:n.*478+16_*478+17del
ENST00000684605.1:n.1619+16_1619+17del
ENST00000684658.1:n.1224+16_1224+17del
ENST00000684715.1:n.1224+16_1224+17del
ENST00000684765.1:c.1079+16_1079+17del	ENSP00000507910.1:n.1079+16_1079+17del
ENST00000336451.8:c.*478+16_*478+17del	ENSP00000336683.4:n.*478+16_*478+17del
ENST00000444024.3:c.1079+16_1079+17del MANE Select	ENSP00000412708.2:n.1079+16_1079+17del
ENST00000622845.5:c.569+16_569+17del	ENSP00000481280.1:n.569+16_569+17del
ENST00000644054.1:c.1002+16_1002+17del
ENST00000644711.1:c.1079+16_1079+17del	ENSP00000494106.1:n.1079+16_1079+17del
ENST00000645367.1:n.1073_1074del
ENST00000645895.1:n.1196+16_1196+17del
ENST00000646926.1:c.422+16_422+17del
ENST00000336451.7:c.446+16_446+17del	ENSP00000336683.3:n.446+16_446+17del
ENST00000367303.8:c.1079+16_1079+17del	ENSP00000356272.4:n.1079+16_1079+17del
ENST00000444024.1:c.569+16_569+17del	ENSP00000412708.1:n.569+16_569+17del
ENST00000622845.4:c.569+16_569+17del	ENSP00000481280.1:n.569+16_569+17del
NM_001271937.1:c.569+16_569+17del	NP_001258866.1:n.569+16_569+17del
NM_017909.3:c.1079+16_1079+17del	NP_060379.2:n.1079+16_1079+17del
XM_005267040.2:c.446+16_446+17del	XP_005267097.1:n.446+16_446+17del
XR_942497.1:n.1259+16_1259+17del
XM_005267040.4:c.446+16_446+17del	XP_005267097.1:n.446+16_446+17del
XM_017010988.2:c.446+16_446+17del	XP_016866477.1:n.446+16_446+17del
XR_001743503.2:n.1247+16_1247+17del
XR_002956288.1:n.1204+16_1204+17del
NM_017909.4:c.1079+16_1079+17del MANE Select	NP_060379.2:n.1079+16_1079+17del
NM_001271937.2:c.569+16_569+17del	NP_001258866.1:n.569+16_569+17del