Canonical Allele Identifier: CA126895
Gene: DPP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.154305155C>T , CM000669.2:g.154305155C>T GRCh38
NC_000007.13:g.154002240C>T , CM000669.1:g.154002240C>T GRCh37
NC_000007.12:g.153633173C>T NCBI36
NG_033878.1:g.422822C>T
NG_033878.2:g.562170C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706130.1:c.61-141059C>T ENSP00000516215.1:n.61-141059C>T
ENST00000377770.8:c.244-141059C>T MANE Select ENSP00000367001.3:n.244-141059C>T
ENST00000332007.7:c.-340C>T ENSP00000328226.3:n.-340C>T
ENST00000377770.7:c.244-141059C>T ENSP00000367001.3:n.244-141059C>T
ENST00000404039.5:c.52-141059C>T ENSP00000385578.1:n.52-141059C>T
ENST00000406326.5:c.244-141059C>T ENSP00000384393.1:n.244-141059C>T
ENST00000462622.5:n.46C>T
NM_001039350.2:c.52-141059C>T NP_001034439.1:n.52-141059C>T
NM_001290253.1:c.244-141059C>T NP_001277182.1:n.244-141059C>T
NM_130797.3:c.244-141059C>T NP_570629.2:n.244-141059C>T
XM_011515865.1:c.52-141059C>T XP_011514167.1:n.52-141059C>T
NM_001364497.1:c.61-141059C>T NP_001351426.1:n.61-141059C>T
NM_001364498.1:c.61-141059C>T NP_001351427.1:n.61-141059C>T
NM_001364499.1:c.61-141059C>T NP_001351428.1:n.61-141059C>T
NM_001364500.1:c.61-141059C>T NP_001351429.1:n.61-141059C>T
NM_001364501.1:c.52-141059C>T NP_001351430.1:n.52-141059C>T
NR_157195.1:n.694-141059C>T
NM_130797.4:c.244-141059C>T MANE Select NP_570629.2:n.244-141059C>T
NM_001039350.3:c.52-141059C>T NP_001034439.1:n.52-141059C>T
NM_001290253.2:c.244-141059C>T NP_001277182.1:n.244-141059C>T
NM_001364497.2:c.61-141059C>T NP_001351426.1:n.61-141059C>T
NM_001364498.2:c.61-141059C>T NP_001351427.1:n.61-141059C>T
NM_001364499.2:c.61-141059C>T NP_001351428.1:n.61-141059C>T
NM_001364500.2:c.61-141059C>T NP_001351429.1:n.61-141059C>T
NM_001364501.2:c.52-141059C>T NP_001351430.1:n.52-141059C>T
NR_157195.2:n.694-141059C>T