Canonical Allele Identifier: CA290086091

Gene: RDM1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35930188G>A , CM000679.2:g.35930188G>A	GRCh38
NC_000017.10:g.34257192G>A , CM000679.1:g.34257192G>A	GRCh37
NC_000017.9:g.31281305G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_145654.4:c.164C>T MANE Select	NP_663629.1:p.Ala55Val
ENST00000620284.5:c.164C>T MANE Select	ENSP00000483549.1:p.Ala55Val
NM_001034836.1:c.164C>T	NP_001030008.1:p.Ala55Val
NM_001034836.2:c.164C>T	NP_001030008.1:p.Ala55Val
NM_001163120.1:c.164C>T	NP_001156592.1:p.Ala55Val
NM_001163120.2:c.164C>T	NP_001156592.1:p.Ala55Val
NM_001163121.1:c.164C>T	NP_001156593.1:p.Ala55Val
NM_001163121.2:c.164C>T	NP_001156593.1:p.Ala55Val
NM_001163122.1:c.95C>T	NP_001156594.1:p.Ala32Val
NM_001163124.1:c.95C>T	NP_001156596.1:p.Ala32Val
NM_001163125.1:c.95C>T	NP_001156597.1:p.Ala32Val
NM_001163130.1:c.95C>T	NP_001156602.1:p.Ala32Val
NM_001330194.1:c.164C>T	NP_001317123.1:p.Ala55Val
NM_001330194.2:c.164C>T	NP_001317123.1:p.Ala55Val
NM_145654.3:c.164C>T	NP_663629.1:p.Ala55Val
NR_027996.1:n.145+444C>T
NR_027996.2:n.142+444C>T
NR_027997.1:n.213C>T
NR_027997.2:n.210C>T
NR_027998.1:n.213C>T
NR_027998.2:n.210C>T
NR_027999.1:n.112C>T
NR_028000.1:n.112C>T
ENST00000612980.4:c.164C>T	ENSP00000483387.1:p.Ala55Val
ENST00000613308.4:c.164C>T	ENSP00000482288.1:p.Ala55Val
ENST00000615024.4:c.95C>T	ENSP00000481648.1:p.Ala32Val
ENST00000615288.4:c.164C>T	ENSP00000477869.1:p.Ala55Val
ENST00000615378.1:c.95C>T	ENSP00000480131.1:p.Ala32Val
ENST00000616596.4:c.164C>T	ENSP00000478915.1:p.Ala55Val
ENST00000617591.4:c.95C>T	ENSP00000479622.1:p.Ala32Val
ENST00000618511.4:c.95C>T	ENSP00000477995.1:p.Ala32Val
ENST00000619193.4:c.164C>T	ENSP00000482981.1:p.Ala55Val
ENST00000619262.4:c.95C>T	ENSP00000479310.1:p.Ala32Val
ENST00000619368.4:c.96+444C>T	ENSP00000478131.1:n.96+444C>T
ENST00000619828.4:c.95C>T	ENSP00000483933.1:p.Ala32Val
ENST00000619876.4:c.95C>T	ENSP00000483890.1:p.Ala32Val
ENST00000620284.4:c.164C>T	ENSP00000483549.1:p.Ala55Val
XM_011524509.1:c.164C>T	XP_011522811.1:p.Ala55Val
XM_011524509.2:c.164C>T	XP_011522811.1:p.Ala55Val
XM_011524510.1:c.164C>T	XP_011522812.1:p.Ala55Val