Canonical Allele Identifier: CA14907188

Gene: PRDM15

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41866243C>G , CM000683.2:g.41866243C>G	GRCh38
NC_000021.8:g.43286352C>G , CM000683.1:g.43286352C>G	GRCh37
NC_000021.7:g.42159421C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269844.5:c.-282+1057G>C	ENSP00000269844.4:n.-282+1057G>C
ENST00000398548.6:c.-9-5871G>C MANE Select	ENSP00000381556.2:n.-9-5871G>C
ENST00000422911.6:c.-9-5871G>C	ENSP00000408592.2:n.-9-5871G>C
ENST00000449395.6:c.-9-5871G>C	ENSP00000396943.2:n.-9-5871G>C
ENST00000269844.4:c.619+1057G>C	ENSP00000269844.3:n.619+1057G>C
ENST00000398548.5:c.103-5871G>C	ENSP00000381556.1:n.103-5871G>C
ENST00000422911.5:c.103-5871G>C	ENSP00000408592.1:n.103-5871G>C
ENST00000433067.5:c.619+1057G>C	ENSP00000415471.1:n.619+1057G>C
ENST00000441787.5:c.-9-5871G>C	ENSP00000387958.1:n.-9-5871G>C
ENST00000449395.5:c.103-5871G>C	ENSP00000396943.1:n.103-5871G>C
NM_001040424.2:c.103-5871G>C	NP_001035514.1:n.103-5871G>C
NM_001282934.1:c.103-5871G>C	NP_001269863.1:n.103-5871G>C
NM_022115.4:c.619+1057G>C	NP_071398.3:n.619+1057G>C
NR_104257.1:n.214-5871G>C
NR_104258.1:n.214-5871G>C
XM_006724039.2:c.103-5871G>C	XP_006724102.1:n.103-5871G>C
XM_006724040.2:c.103-5871G>C	XP_006724103.1:n.103-5871G>C
XM_011529672.1:c.4-5871G>C	XP_011527974.1:n.4-5871G>C
XM_011529673.1:c.4-5871G>C	XP_011527975.1:n.4-5871G>C
XM_011529674.1:c.103-5871G>C	XP_011527976.1:n.103-5871G>C
XM_011529675.1:c.-9-5871G>C	XP_011527977.1:n.-9-5871G>C
XM_011529676.1:c.-9-5871G>C	XP_011527978.1:n.-9-5871G>C
XM_011529678.1:c.-9-5871G>C	XP_011527980.1:n.-9-5871G>C
XM_011529680.1:c.-9-5871G>C	XP_011527982.1:n.-9-5871G>C
XM_011529681.1:c.4-5871G>C	XP_011527983.1:n.4-5871G>C
XM_011529682.1:c.103-5871G>C	XP_011527984.1:n.103-5871G>C
XM_011529683.1:c.619+1057G>C	XP_011527985.1:n.619+1057G>C
XR_937542.1:n.128-5871G>C
NR_135464.1:n.210-5871G>C
XM_011529676.2:c.-9-5871G>C	XP_011527978.1:n.-9-5871G>C
XM_011529678.2:c.-9-5871G>C	XP_011527980.1:n.-9-5871G>C
XM_011529681.3:c.4-5871G>C	XP_011527983.1:n.4-5871G>C
XM_017028425.1:c.-9-5871G>C	XP_016883914.1:n.-9-5871G>C
XM_017028426.1:c.-9-5871G>C	XP_016883915.1:n.-9-5871G>C
XR_001754886.1:n.103-5871G>C
XR_001754887.1:n.103-5871G>C
NM_001040424.3:c.-9-5871G>C MANE Select	NP_001035514.2:n.-9-5871G>C
NM_001282934.2:c.-9-5871G>C	NP_001269863.2:n.-9-5871G>C
NM_022115.5:c.268+1057G>C	NP_071398.4:n.268+1057G>C
NR_104257.2:n.76-5871G>C
NR_104258.2:n.76-5871G>C
NR_135464.2:n.72-5871G>C
NM_022115.7:c.-282+1057G>C	NP_071398.5:n.-282+1057G>C