Canonical Allele Identifier: CA3061541

Gene: PRDM5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.120922573C>A , CM000666.2:g.120922573C>A	GRCh38
NC_000004.11:g.121843728C>A , CM000666.1:g.121843728C>A	GRCh37
NC_000004.10:g.122063178C>A	NCBI36
NG_031862.2:g.5286G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018699.4:c.36G>T MANE Select	NP_061169.2:p.Leu12=
ENST00000264808.8:c.36G>T MANE Select	ENSP00000264808.3:p.Leu12=
NM_001300823.1:c.36G>T	NP_001287752.1:p.Leu12=
NM_001300823.2:c.36G>T	NP_001287752.1:p.Leu12=
NM_001300824.1:c.36G>T	NP_001287753.1:p.Leu12=
NM_001300824.2:c.36G>T	NP_001287753.1:p.Leu12=
NM_001379104.1:c.36G>T	NP_001366033.1:p.Leu12=
NM_001379106.1:c.36G>T	NP_001366035.1:p.Leu12=
NM_018699.3:c.36G>T	NP_061169.2:p.Leu12=
ENST00000264808.7:c.36G>T	ENSP00000264808.3:p.Leu12=
ENST00000394435.2:c.36G>T	ENSP00000377955.2:p.Leu12=
ENST00000428209.6:c.36G>T	ENSP00000404832.2:p.Leu12=
ENST00000505033.1:n.154G>T
ENST00000505484.5:n.109G>T
ENST00000512845.5:n.123G>T
ENST00000515109.5:c.36G>T	ENSP00000422309.1:p.Leu12=
XM_005262708.2:c.36G>T	XP_005262765.1:p.Leu12=
XM_005262708.3:c.36G>T	XP_005262765.1:p.Leu12=
XM_011531562.1:c.36G>T	XP_011529864.1:p.Leu12=
XM_011531562.2:c.36G>T	XP_011529864.1:p.Leu12=
XM_011531563.1:c.36G>T	XP_011529865.1:p.Leu12=
XM_011531563.2:c.36G>T	XP_011529865.1:p.Leu12=
XM_011531564.1:c.36G>T	XP_011529866.1:p.Leu12=
XM_011531564.2:c.36G>T	XP_011529866.1:p.Leu12=
XM_011531565.1:c.36G>T	XP_011529867.1:p.Leu12=
XM_011531565.2:c.36G>T	XP_011529867.1:p.Leu12=
XM_011531566.1:c.36G>T	XP_011529868.1:p.Leu12=
XM_011531566.3:c.36G>T	XP_011529868.1:p.Leu12=
XM_011531567.1:c.36G>T	XP_011529869.1:p.Leu12=
XM_011531567.2:c.36G>T	XP_011529869.1:p.Leu12=
XM_011531568.1:c.36G>T	XP_011529870.1:p.Leu12=
XM_011531568.2:c.36G>T	XP_011529870.1:p.Leu12=
XM_011531569.1:c.36G>T	XP_011529871.1:p.Leu12=
XM_011531569.3:c.36G>T	XP_011529871.1:p.Leu12=
XM_011531570.1:c.-464G>T	XP_011529872.1:n.-464G>T
XM_011531570.3:c.-464G>T	XP_011529872.1:n.-464G>T
XM_017007669.1:c.36G>T	XP_016863158.1:p.Leu12=
XM_017007670.1:c.36G>T	XP_016863159.1:p.Leu12=
XM_024453879.1:c.-464G>T	XP_024309647.1:n.-464G>T
XR_938677.1:n.277G>T
XR_938677.3:n.277G>T
XR_938678.1:n.277G>T
XR_938679.1:n.277G>T
XR_938680.1:n.277G>T
XR_938680.2:n.277G>T