Canonical Allele Identifier: CA1154667668

Gene: PRDM2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.13813331C>A , CM000663.2:g.13813331C>A	GRCh38
NC_000001.10:g.14139826C>A , CM000663.1:g.14139826C>A	GRCh37
NC_000001.9:g.14012413C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311066.10:c.5037-3096C>A MANE Select	ENSP00000312352.6:n.5037-3096C>A
ENST00000235372.11:c.5037-3096C>A	ENSP00000235372.6:n.5037-3096C>A
ENST00000376048.9:c.512-3096C>A	ENSP00000365216.5:n.512-3096C>A
ENST00000503842.5:c.20-3096C>A	ENSP00000425028.1:n.20-3096C>A
ENST00000505823.5:c.20-3096C>A	ENSP00000426737.1:n.20-3096C>A
NM_001135610.1:c.512-3096C>A	NP_001129082.1:n.512-3096C>A
NM_012231.4:c.5037-3096C>A	NP_036363.2:n.5037-3096C>A
XM_011542092.1:c.4499-3096C>A	XP_011540394.1:n.4499-3096C>A
XM_011542093.1:c.542-3096C>A	XP_011540395.1:n.542-3096C>A
XM_017002255.1:c.5037-3096C>A	XP_016857744.1:n.5037-3096C>A
XM_017002256.1:c.5037-3096C>A	XP_016857745.1:n.5037-3096C>A
XM_017002259.2:c.4434-3096C>A	XP_016857748.1:n.4434-3096C>A
XM_017002260.2:c.4434-3096C>A	XP_016857749.1:n.4434-3096C>A
XM_017002261.2:c.4434-3096C>A	XP_016857750.1:n.4434-3096C>A
XM_017002263.2:c.4434-3096C>A	XP_016857752.1:n.4434-3096C>A
XM_017002264.2:c.764-3096C>A	XP_016857753.1:n.764-3096C>A
XR_002957562.1:n.4619-3096C>A
NM_001135610.2:c.512-3096C>A	NP_001129082.1:n.512-3096C>A
NM_001393986.1:c.5037-3096C>A MANE Select	NP_001380915.1:n.5037-3096C>A
NM_001393987.1:c.4434-3096C>A	NP_001380916.1:n.4434-3096C>A
NM_012231.5:c.5037-3096C>A	NP_036363.2:n.5037-3096C>A