Canonical Allele Identifier: CA256734

Gene: RDX

Linked Data

• ClinVar Variation Id: 13186
• ClinVar RCV Id: RCV000014074
• dbSNP Id: rs121918380
• MyVariant Identifiers: chr11:g.110134689G>A (hg19) ; chr11:g.110263964G>A (hg38)
• PubMed: PMID:17226784

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110263964G>A , CM000673.2:g.110263964G>A	GRCh38
NC_000011.9:g.110134689G>A , CM000673.1:g.110134689G>A	GRCh37
NC_000011.8:g.109639899G>A	NCBI36
NG_023044.1:g.37749C>T
NG_023044.2:g.37749C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000642511.1:c.317C>T
ENST00000645495.2:c.463C>T MANE Select	ENSP00000496503.2:p.Gln155Ter
ENST00000645527.1:c.463C>T	ENSP00000496121.1:p.Gln155Ter
ENST00000646663.1:c.463C>T	ENSP00000494693.1:p.Gln155Ter
ENST00000647231.1:c.463C>T	ENSP00000496414.1:p.Gln155Ter
ENST00000343115.8:c.463C>T	ENSP00000342830.4:p.Gln155Ter
ENST00000405097.5:c.463C>T	ENSP00000384136.1:p.Gln155Ter
ENST00000528498.5:c.463C>T	ENSP00000432112.1:p.Gln155Ter
ENST00000528556.5:c.*451C>T	ENSP00000434881.1:n.*451C>T
ENST00000528900.5:c.-83+15717C>T	ENSP00000433580.1:n.-83+15717C>T
ENST00000530131.5:c.97-5775C>T	ENSP00000432829.1:n.97-5775C>T
ENST00000530301.5:c.367C>T	ENSP00000436277.1:p.Gln123Ter
ENST00000530749.5:c.463C>T	ENSP00000437301.1:p.Gln155Ter
ENST00000532118.5:c.430C>T	ENSP00000437140.1:p.Gln144Ter
ENST00000534683.1:c.-81C>T	ENSP00000431560.1:n.-81C>T
ENST00000544551.5:c.60-5775C>T	ENSP00000445826.1:n.60-5775C>T
NM_001260492.1:c.463C>T	NP_001247421.1:p.Gln155Ter
NM_001260493.1:c.463C>T	NP_001247422.1:p.Gln155Ter
NM_001260494.1:c.60-5775C>T	NP_001247423.1:n.60-5775C>T
NM_001260495.1:c.-83+15717C>T	NP_001247424.1:n.-83+15717C>T
NM_001260496.1:c.367C>T	NP_001247425.1:p.Gln123Ter
NM_002906.3:c.463C>T	NP_002897.1:p.Gln155Ter
NM_001260492.2:c.463C>T	NP_001247421.1:p.Gln155Ter
NM_002906.4:c.463C>T MANE Select	NP_002897.1:p.Gln155Ter
NM_001260493.2:c.463C>T	NP_001247422.1:p.Gln155Ter
NM_001260494.2:c.60-5775C>T	NP_001247423.1:n.60-5775C>T
NM_001260495.2:c.-83+15717C>T	NP_001247424.1:n.-83+15717C>T
NM_001260496.2:c.367C>T	NP_001247425.1:p.Gln123Ter