Canonical Allele Identifier: CA387785021

Gene: PDS5B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32706974G>A , CM000675.2:g.32706974G>A	GRCh38
NC_000013.10:g.33281111G>A , CM000675.1:g.33281111G>A	GRCh37
NC_000013.9:g.32179111G>A	NCBI36
NG_021308.1:g.125548G>A
NG_021308.2:g.125548G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015032.4:c.1897G>A MANE Select	NP_055847.1:p.Ala633Thr
ENST00000315596.15:c.1897G>A MANE Select	ENSP00000313851.10:p.Ala633Thr
NM_015032.3:c.1897G>A	NP_055847.1:p.Ala633Thr
ENST00000315596.14:c.1897G>A	ENSP00000313851.10:p.Ala633Thr
ENST00000450460.5:c.1897G>A	ENSP00000401619.1:p.Ala633Thr
ENST00000481616.1:n.496G>A
XM_005266298.3:c.1897G>A	XP_005266355.1:p.Ala633Thr
XM_005266298.4:c.1897G>A	XP_005266355.1:p.Ala633Thr
XM_011534999.1:c.1897G>A	XP_011533301.1:p.Ala633Thr
XM_011534999.2:c.1897G>A	XP_011533301.1:p.Ala633Thr
XM_011535000.1:c.1897G>A	XP_011533302.1:p.Ala633Thr
XM_011535000.2:c.1897G>A	XP_011533302.1:p.Ala633Thr
XM_011535001.1:c.1897G>A	XP_011533303.1:p.Ala633Thr
XM_011535002.1:c.1069G>A	XP_011533304.1:p.Ala357Thr
XM_011535002.3:c.1069G>A	XP_011533304.1:p.Ala357Thr
XM_017020448.1:c.1897G>A	XP_016875937.1:p.Ala633Thr
XM_017020449.1:c.1897G>A	XP_016875938.1:p.Ala633Thr
XM_017020450.1:c.1897G>A	XP_016875939.1:p.Ala633Thr
XM_017020451.1:c.1897G>A	XP_016875940.1:p.Ala633Thr
XM_017020452.2:c.1897G>A	XP_016875941.1:p.Ala633Thr
XM_017020453.1:c.1897G>A	XP_016875942.1:p.Ala633Thr