Canonical Allele Identifier: CA6943295

Gene: PDS5B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32742684A>G , CM000675.2:g.32742684A>G	GRCh38
NC_000013.10:g.33316822A>G , CM000675.1:g.33316822A>G	GRCh37
NC_000013.9:g.32214822A>G	NCBI36
NG_021308.1:g.161259A>G
NG_021308.2:g.161258A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315596.15:c.2569A>G MANE Select	ENSP00000313851.10:p.Ile857Val
ENST00000315596.14:c.2569A>G	ENSP00000313851.10:p.Ile857Val
ENST00000450460.5:c.2569A>G	ENSP00000401619.1:p.Ile857Val
NM_015032.3:c.2569A>G	NP_055847.1:p.Ile857Val
XM_005266298.3:c.2569A>G	XP_005266355.1:p.Ile857Val
XM_011534999.1:c.2569A>G	XP_011533301.1:p.Ile857Val
XM_011535000.1:c.2569A>G	XP_011533302.1:p.Ile857Val
XM_011535001.1:c.2569A>G	XP_011533303.1:p.Ile857Val
XM_011535002.1:c.1741A>G	XP_011533304.1:p.Ile581Val
XM_005266298.4:c.2569A>G	XP_005266355.1:p.Ile857Val
XM_011534999.2:c.2569A>G	XP_011533301.1:p.Ile857Val
XM_011535000.2:c.2569A>G	XP_011533302.1:p.Ile857Val
XM_011535002.3:c.1741A>G	XP_011533304.1:p.Ile581Val
XM_017020448.1:c.2569A>G	XP_016875937.1:p.Ile857Val
XM_017020449.1:c.2569A>G	XP_016875938.1:p.Ile857Val
XM_017020450.1:c.2569A>G	XP_016875939.1:p.Ile857Val
XM_017020451.1:c.2569A>G	XP_016875940.1:p.Ile857Val
XM_017020452.2:c.2569A>G	XP_016875941.1:p.Ile857Val
XM_017020453.1:c.2569A>G	XP_016875942.1:p.Ile857Val
NM_015032.4:c.2569A>G MANE Select	NP_055847.1:p.Ile857Val