Canonical Allele Identifier: CA2838366342
Gene: PRDM6 HGNC NCBI
PRDM6-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.123090166_123090168dup , CM000667.2:g.123090166_123090168dup GRCh38
NC_000005.9:g.122425861_122425863dup , CM000667.1:g.122425861_122425863dup GRCh37
NC_000005.8:g.122453760_122453762dup NCBI36
NG_053114.1:g.6064_6066dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000407847.5:c.152_154dup (PRDM6) MANE Select ENSP00000384725.3:p.Gln51_Pro52insGln
ENST00000407847.4:c.152_154dup (PRDM6) ENSP00000384725.3:p.Gln51_Pro52insGln
NM_001136239.1:c.152_154dup (PRDM6) NP_001129711.1:p.Gln51_Pro52insGln
XM_005272128.3:c.152_154dup (PRDM6) XP_005272185.1:p.Gln51_Pro52insGln
XM_011543725.1:c.197-9488_197-9486dup (PRDM6) XP_011542027.1:n.197-9488_197-9486dup
XR_948304.1:n.539_541dup (PRDM6)
XR_948305.1:n.539_541dup (PRDM6)
NM_001136239.3:c.152_154dup (PRDM6) NP_001129711.1:p.Gln51_Pro52insGln
NR_146771.1:n.150_152dup (PRDM6-AS1)
XR_001742346.1:n.539_541dup (PRDM6)
NM_001136239.4:c.152_154dup (PRDM6) MANE Select NP_001129711.1:p.Gln51_Pro52insGln