Canonical Allele Identifier: CA372007974

Gene: RAD21

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116858402G>A , CM000670.2:g.116858402G>A	GRCh38
NC_000008.10:g.117870641G>A , CM000670.1:g.117870641G>A	GRCh37
NC_000008.9:g.117939822G>A	NCBI36
NG_032862.1:g.21465C>T , LRG_772:g.21465C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006265.3:c.431C>T MANE Select	NP_006256.1:p.Thr144Ile
ENST00000297338.7:c.431C>T MANE Select	ENSP00000297338.2:p.Thr144Ile
NM_006265.2:c.431C>T , LRG_772t1:c.431C>T	NP_006256.1:p.Thr144Ile
ENST00000297338.6:c.431C>T	ENSP00000297338.2:p.Thr144Ile
ENST00000517485.5:c.431C>T	ENSP00000427923.1:p.Thr144Ile
ENST00000517485.6:c.431C>T	ENSP00000427923.2:p.Thr144Ile
ENST00000517749.2:c.431C>T	ENSP00000430273.2:p.Thr144Ile
ENST00000519837.6:c.431C>T	ENSP00000430524.2:p.Thr144Ile
ENST00000520992.5:c.431C>T	ENSP00000429342.1:p.Thr144Ile
ENST00000520992.6:c.431C>T	ENSP00000429342.2:p.Thr144Ile
ENST00000522699.2:c.431C>T	ENSP00000428158.2:p.Thr144Ile
ENST00000523547.1:n.673C>T
ENST00000523547.2:n.541C>T
ENST00000685972.1:n.514C>T
ENST00000686622.1:n.528C>T
ENST00000687122.1:n.3259C>T
ENST00000687358.1:c.431C>T	ENSP00000509687.1:p.Thr144Ile
ENST00000687902.1:c.431C>T	ENSP00000510729.1:p.Thr144Ile
ENST00000688033.1:n.501C>T
ENST00000689124.1:n.645C>T
ENST00000689504.1:n.541C>T
ENST00000690166.1:n.331C>T
ENST00000690189.1:n.2246C>T