Canonical Allele Identifier: CA671601826

Gene: RDX

Linked Data

• dbSNP Id: rs1160374157
• gnomAD v3: 11-110263895-TTTTA-T
• gnomAD v4: 11-110263895-TTTTA-T
• MyVariant Identifiers: chr11:g.110134621_110134624del (hg19) ; chr11:g.110263896_110263899del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110263901_110263904del , CM000673.2:g.110263901_110263904del	GRCh38
NC_000011.9:g.110134626_110134629del , CM000673.1:g.110134626_110134629del	GRCh37
NC_000011.8:g.109639836_109639839del	NCBI36
NG_023044.1:g.37814_37817del
NG_023044.2:g.37814_37817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642511.1:c.321+61_321+64del
ENST00000645495.2:c.467+61_467+64del MANE Select	ENSP00000496503.2:n.467+61_467+64del
ENST00000645527.1:c.467+61_467+64del	ENSP00000496121.1:n.467+61_467+64del
ENST00000646663.1:c.467+61_467+64del	ENSP00000494693.1:n.467+61_467+64del
ENST00000647231.1:c.467+61_467+64del	ENSP00000496414.1:n.467+61_467+64del
ENST00000343115.8:c.467+61_467+64del	ENSP00000342830.4:n.467+61_467+64del
ENST00000405097.5:c.467+61_467+64del	ENSP00000384136.1:n.467+61_467+64del
ENST00000528498.5:c.467+61_467+64del	ENSP00000432112.1:n.467+61_467+64del
ENST00000528900.5:c.-83+15782_-83+15785del	ENSP00000433580.1:n.-83+15782_-83+15785del
ENST00000530131.5:c.97-5710_97-5707del	ENSP00000432829.1:n.97-5710_97-5707del
ENST00000530301.5:c.371+61_371+64del	ENSP00000436277.1:n.371+61_371+64del
ENST00000530749.5:c.467+61_467+64del	ENSP00000437301.1:n.467+61_467+64del
ENST00000532118.5:c.434+61_434+64del	ENSP00000437140.1:n.434+61_434+64del
ENST00000534683.1:c.-77+61_-77+64del	ENSP00000431560.1:n.-77+61_-77+64del
ENST00000544551.5:c.60-5710_60-5707del	ENSP00000445826.1:n.60-5710_60-5707del
NM_001260492.1:c.467+61_467+64del	NP_001247421.1:n.467+61_467+64del
NM_001260493.1:c.467+61_467+64del	NP_001247422.1:n.467+61_467+64del
NM_001260494.1:c.60-5710_60-5707del	NP_001247423.1:n.60-5710_60-5707del
NM_001260495.1:c.-83+15782_-83+15785del	NP_001247424.1:n.-83+15782_-83+15785del
NM_001260496.1:c.371+61_371+64del	NP_001247425.1:n.371+61_371+64del
NM_002906.3:c.467+61_467+64del	NP_002897.1:n.467+61_467+64del
NM_001260492.2:c.467+61_467+64del	NP_001247421.1:n.467+61_467+64del
NM_002906.4:c.467+61_467+64del MANE Select	NP_002897.1:n.467+61_467+64del
NM_001260493.2:c.467+61_467+64del	NP_001247422.1:n.467+61_467+64del
NM_001260494.2:c.60-5710_60-5707del	NP_001247423.1:n.60-5710_60-5707del
NM_001260495.2:c.-83+15782_-83+15785del	NP_001247424.1:n.-83+15782_-83+15785del
NM_001260496.2:c.371+61_371+64del	NP_001247425.1:n.371+61_371+64del