Canonical Allele Identifier: CA6943717

Gene: PDS5B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32770695C>G , CM000675.2:g.32770695C>G	GRCh38
NC_000013.10:g.33344833C>G , CM000675.1:g.33344833C>G	GRCh37
NC_000013.9:g.32242833C>G	NCBI36
NG_021308.1:g.189270C>G
NG_021308.2:g.189269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315596.15:c.4106C>G MANE Select	ENSP00000313851.10:p.Ser1369Cys
ENST00000315596.14:c.4106C>G	ENSP00000313851.10:p.Ser1369Cys
ENST00000450460.5:c.4106C>G	ENSP00000401619.1:p.Ser1369Cys
ENST00000474274.1:n.413C>G
NM_015032.3:c.4106C>G	NP_055847.1:p.Ser1369Cys
XM_005266298.3:c.4109C>G	XP_005266355.1:p.Ser1370Cys
XM_011534999.1:c.4103C>G	XP_011533301.1:p.Ser1368Cys
XM_011535000.1:c.4100C>G	XP_011533302.1:p.Ser1367Cys
XM_011535001.1:c.4064+135C>G	XP_011533303.1:n.4064+135C>G
XM_011535002.1:c.3281C>G	XP_011533304.1:p.Ser1094Cys
XM_005266298.4:c.4109C>G	XP_005266355.1:p.Ser1370Cys
XM_011534999.2:c.4103C>G	XP_011533301.1:p.Ser1368Cys
XM_011535000.2:c.4100C>G	XP_011533302.1:p.Ser1367Cys
XM_011535002.3:c.3281C>G	XP_011533304.1:p.Ser1094Cys
XM_017020448.1:c.4109C>G	XP_016875937.1:p.Ser1370Cys
XM_017020449.1:c.4109C>G	XP_016875938.1:p.Ser1370Cys
XM_017020450.1:c.4106C>G	XP_016875939.1:p.Ser1369Cys
XM_017020451.1:c.4103C>G	XP_016875940.1:p.Ser1368Cys
XM_017020452.2:c.4064+135C>G	XP_016875941.1:n.4064+135C>G
XM_017020453.1:c.4058+135C>G	XP_016875942.1:n.4058+135C>G
NM_015032.4:c.4106C>G MANE Select	NP_055847.1:p.Ser1369Cys