Canonical Allele Identifier: CA13519127

Gene: PRDM11

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45229181A>C , CM000673.2:g.45229181A>C	GRCh38
NC_000011.9:g.45250732A>C , CM000673.1:g.45250732A>C	GRCh37
NC_000011.8:g.45207308A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001384648.1:c.*1022A>C MANE Select	NP_001371577.1:n.*1022A>C
ENST00000683152.1:c.*1022A>C MANE Select	ENSP00000507575.1:n.*1022A>C
NM_001256695.1:c.*1022A>C	NP_001243624.1:n.*1022A>C
NM_001256695.2:c.*1022A>C	NP_001243624.1:n.*1022A>C
ENST00000622142.4:c.*1022A>C	ENSP00000480626.1:n.*1022A>C
ENST00000622142.5:c.*1022A>C	ENSP00000480626.1:n.*1022A>C
XM_011520222.1:c.*1022A>C	XP_011518524.1:n.*1022A>C
XM_011520222.2:c.*1022A>C	XP_011518524.1:n.*1022A>C
XM_011520223.1:c.*1022A>C	XP_011518525.1:n.*1022A>C
XM_011520223.2:c.*1022A>C	XP_011518525.1:n.*1022A>C
XM_011520224.1:c.*1022A>C	XP_011518526.1:n.*1022A>C
XM_011520224.3:c.*1022A>C	XP_011518526.1:n.*1022A>C
XM_011520225.1:c.*1022A>C	XP_011518527.1:n.*1022A>C
XM_011520225.2:c.*1022A>C	XP_011518527.1:n.*1022A>C
XM_011520226.1:c.*1022A>C	XP_011518528.1:n.*1022A>C
XM_011520226.2:c.*1022A>C	XP_011518528.1:n.*1022A>C
XM_011520227.1:c.*1022A>C	XP_011518529.1:n.*1022A>C
XM_011520227.2:c.*1022A>C	XP_011518529.1:n.*1022A>C
XM_011520228.1:c.*1022A>C	XP_011518530.1:n.*1022A>C
XM_011520228.3:c.*1022A>C	XP_011518530.1:n.*1022A>C
XM_011520229.1:c.*1022A>C	XP_011518531.1:n.*1022A>C
XR_930882.1:n.4325+662A>C