Canonical Allele Identifier: CA2390501761

Gene: PRDM15

Linked Data

• dbSNP Id: rs7279297

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41807559A>T , CM000683.2:g.41807559A>T	GRCh38
NC_000021.8:g.43227915A>T , CM000683.1:g.43227915A>T	GRCh37
NC_000021.7:g.42100984A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000269844.5:c.2850+2595T>A	ENSP00000269844.4:n.2850+2595T>A
ENST00000398548.6:c.2652+2595T>A MANE Select	ENSP00000381556.2:n.2652+2595T>A
ENST00000422911.6:c.2712+2595T>A	ENSP00000408592.2:n.2712+2595T>A
ENST00000449395.6:c.*1103+2595T>A	ENSP00000396943.2:n.*1103+2595T>A
ENST00000269844.4:c.3750+2595T>A	ENSP00000269844.3:n.3750+2595T>A
ENST00000398548.5:c.2763+2595T>A	ENSP00000381556.1:n.2763+2595T>A
ENST00000422911.5:c.2823+2595T>A	ENSP00000408592.1:n.2823+2595T>A
ENST00000433067.5:c.3750+2595T>A	ENSP00000415471.1:n.3750+2595T>A
ENST00000441787.5:c.*1103+2595T>A	ENSP00000387958.1:n.*1103+2595T>A
ENST00000447016.6:c.2652+2595T>A	ENSP00000431410.1:n.2652+2595T>A
ENST00000447207.6:c.2652+2595T>A	ENSP00000390245.2:n.2652+2595T>A
ENST00000449395.5:c.*1103+2595T>A	ENSP00000396943.1:n.*1103+2595T>A
ENST00000470586.5:n.313+2595T>A
ENST00000486812.5:n.4809+2595T>A
ENST00000495217.1:n.594+2595T>A
NM_001040424.2:c.2763+2595T>A	NP_001035514.1:n.2763+2595T>A
NM_001282934.1:c.2823+2595T>A	NP_001269863.1:n.2823+2595T>A
NM_022115.4:c.3750+2595T>A	NP_071398.3:n.3750+2595T>A
NR_104257.1:n.2882+2595T>A
NR_104258.1:n.2762+2595T>A
NR_104260.1:n.2729+2595T>A
XM_006724039.2:c.2691+2595T>A	XP_006724102.1:n.2691+2595T>A
XM_006724040.2:c.2631+2595T>A	XP_006724103.1:n.2631+2595T>A
XM_011529671.1:c.2727+2595T>A	XP_011527973.1:n.2727+2595T>A
XM_011529672.1:c.2724+2595T>A	XP_011527974.1:n.2724+2595T>A
XM_011529673.1:c.2724+2595T>A	XP_011527975.1:n.2724+2595T>A
XM_011529674.1:c.2721+2595T>A	XP_011527976.1:n.2721+2595T>A
XM_011529675.1:c.2712+2595T>A	XP_011527977.1:n.2712+2595T>A
XM_011529676.1:c.2712+2595T>A	XP_011527978.1:n.2712+2595T>A
XM_011529677.1:c.2712+2595T>A	XP_011527979.1:n.2712+2595T>A
XM_011529678.1:c.2712+2595T>A	XP_011527980.1:n.2712+2595T>A
XM_011529679.1:c.2712+2595T>A	XP_011527981.1:n.2712+2595T>A
XM_011529680.1:c.2712+2595T>A	XP_011527982.1:n.2712+2595T>A
XM_011529681.1:c.2724+2595T>A	XP_011527983.1:n.2724+2595T>A
XM_011529683.1:c.3552+2595T>A	XP_011527985.1:n.3552+2595T>A
XR_937542.1:n.2589-2945T>A
NR_135464.1:n.2870+2595T>A
XM_011529676.2:c.2712+2595T>A	XP_011527978.1:n.2712+2595T>A
XM_011529677.2:c.2712+2595T>A	XP_011527979.1:n.2712+2595T>A
XM_011529678.2:c.2712+2595T>A	XP_011527980.1:n.2712+2595T>A
XM_011529679.2:c.2712+2595T>A	XP_011527981.1:n.2712+2595T>A
XM_011529681.3:c.2724+2595T>A	XP_011527983.1:n.2724+2595T>A
XM_017028425.1:c.2652+2595T>A	XP_016883914.1:n.2652+2595T>A
XM_017028426.1:c.2652+2595T>A	XP_016883915.1:n.2652+2595T>A
XR_001754886.1:n.2823+2595T>A
XR_001754887.1:n.2823+2595T>A
NM_001040424.3:c.2652+2595T>A MANE Select	NP_001035514.2:n.2652+2595T>A
NM_001282934.2:c.2712+2595T>A	NP_001269863.2:n.2712+2595T>A
NM_022115.5:c.3399+2595T>A	NP_071398.4:n.3399+2595T>A
NR_104257.2:n.2744+2595T>A
NR_104258.2:n.2624+2595T>A
NR_135464.2:n.2732+2595T>A
NM_022115.7:c.2850+2595T>A	NP_071398.5:n.2850+2595T>A