Canonical Allele Identifier: CA105128572

Gene: PRDM5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.120880635G>T , CM000666.2:g.120880635G>T	GRCh38
NC_000004.11:g.121801790G>T , CM000666.1:g.121801790G>T	GRCh37
NC_000004.10:g.122021240G>T	NCBI36
NG_031862.2:g.47224C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264808.8:c.177+26839C>A MANE Select	ENSP00000264808.3:n.177+26839C>A
ENST00000264808.7:c.177+26839C>A	ENSP00000264808.3:n.177+26839C>A
ENST00000394435.2:c.177+26839C>A	ENSP00000377955.2:n.177+26839C>A
ENST00000428209.6:c.177+26839C>A	ENSP00000404832.2:n.177+26839C>A
ENST00000505484.5:n.250+26839C>A
ENST00000512845.5:n.264+26839C>A
ENST00000515109.5:c.177+26839C>A	ENSP00000422309.1:n.177+26839C>A
NM_001300823.1:c.177+26839C>A	NP_001287752.1:n.177+26839C>A
NM_001300824.1:c.177+26839C>A	NP_001287753.1:n.177+26839C>A
NM_018699.3:c.177+26839C>A	NP_061169.2:n.177+26839C>A
XM_005262708.2:c.177+26839C>A	XP_005262765.1:n.177+26839C>A
XM_011531562.1:c.177+26839C>A	XP_011529864.1:n.177+26839C>A
XM_011531563.1:c.177+26839C>A	XP_011529865.1:n.177+26839C>A
XM_011531564.1:c.177+26839C>A	XP_011529866.1:n.177+26839C>A
XM_011531565.1:c.177+26839C>A	XP_011529867.1:n.177+26839C>A
XM_011531566.1:c.177+26839C>A	XP_011529868.1:n.177+26839C>A
XM_011531567.1:c.177+26839C>A	XP_011529869.1:n.177+26839C>A
XM_011531568.1:c.177+26839C>A	XP_011529870.1:n.177+26839C>A
XM_011531569.1:c.177+26839C>A	XP_011529871.1:n.177+26839C>A
XM_011531570.1:c.-323+26839C>A	XP_011529872.1:n.-323+26839C>A
XR_938677.1:n.418+26839C>A
XR_938678.1:n.418+26839C>A
XR_938679.1:n.418+26839C>A
XR_938680.1:n.418+26839C>A
XM_005262708.3:c.177+26839C>A	XP_005262765.1:n.177+26839C>A
XM_011531562.2:c.177+26839C>A	XP_011529864.1:n.177+26839C>A
XM_011531563.2:c.177+26839C>A	XP_011529865.1:n.177+26839C>A
XM_011531564.2:c.177+26839C>A	XP_011529866.1:n.177+26839C>A
XM_011531565.2:c.177+26839C>A	XP_011529867.1:n.177+26839C>A
XM_011531566.3:c.177+26839C>A	XP_011529868.1:n.177+26839C>A
XM_011531567.2:c.177+26839C>A	XP_011529869.1:n.177+26839C>A
XM_011531568.2:c.177+26839C>A	XP_011529870.1:n.177+26839C>A
XM_011531569.3:c.177+26839C>A	XP_011529871.1:n.177+26839C>A
XM_011531570.3:c.-323+26839C>A	XP_011529872.1:n.-323+26839C>A
XM_017007668.2:c.99+26839C>A	XP_016863157.1:n.99+26839C>A
XM_017007669.1:c.177+26839C>A	XP_016863158.1:n.177+26839C>A
XM_017007670.1:c.177+26839C>A	XP_016863159.1:n.177+26839C>A
XM_024453879.1:c.-323+26839C>A	XP_024309647.1:n.-323+26839C>A
XR_938677.3:n.418+26839C>A
XR_938680.2:n.418+26839C>A
NM_001300823.2:c.177+26839C>A	NP_001287752.1:n.177+26839C>A
NM_001300824.2:c.177+26839C>A	NP_001287753.1:n.177+26839C>A
NM_001379104.1:c.177+26839C>A	NP_001366033.1:n.177+26839C>A
NM_001379106.1:c.177+26839C>A	NP_001366035.1:n.177+26839C>A
NM_018699.4:c.177+26839C>A MANE Select	NP_061169.2:n.177+26839C>A