Canonical Allele Identifier: CA2579072873
Gene: DPP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.154853871_154853877del , CM000669.2:g.154853871_154853877del GRCh38
NC_000007.13:g.154645581_154645587del , CM000669.1:g.154645581_154645587del GRCh37
NC_000007.12:g.154276514_154276520del NCBI36
NG_033878.1:g.971538_971544del
NG_033878.2:g.1110886_1110892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706130.1:c.1531+44_1531+50del ENSP00000516215.1:n.1531+44_1531+50del
ENST00000706151.1:c.739+44_739+50del ENSP00000516234.1:n.739+44_739+50del
ENST00000706153.1:n.1360+44_1360+50del
ENST00000706154.1:n.998+44_998+50del
ENST00000706155.1:n.1145+44_1145+50del
ENST00000377770.8:c.1714+44_1714+50del MANE Select ENSP00000367001.3:n.1714+44_1714+50del
ENST00000332007.7:c.1528+44_1528+50del ENSP00000328226.3:n.1528+44_1528+50del
ENST00000377770.7:c.1714+44_1714+50del ENSP00000367001.3:n.1714+44_1714+50del
ENST00000404039.5:c.1522+44_1522+50del ENSP00000385578.1:n.1522+44_1522+50del
ENST00000427557.1:c.1393+44_1393+50del ENSP00000397303.1:n.1393+44_1393+50del
ENST00000493268.1:n.279+44_279+50del
NM_001039350.2:c.1522+44_1522+50del NP_001034439.1:n.1522+44_1522+50del
NM_001290252.1:c.1393+44_1393+50del NP_001277181.1:n.1393+44_1393+50del
NM_001936.4:c.1528+44_1528+50del NP_001927.3:n.1528+44_1528+50del
NM_130797.3:c.1714+44_1714+50del NP_570629.2:n.1714+44_1714+50del
XM_011515865.1:c.1522+44_1522+50del XP_011514167.1:n.1522+44_1522+50del
XM_011515866.1:c.1090+44_1090+50del XP_011514168.1:n.1090+44_1090+50del
XR_928190.1:n.154+11437_154+11443del
NM_001364497.1:c.1531+44_1531+50del NP_001351426.1:n.1531+44_1531+50del
NM_001364498.1:c.1531+44_1531+50del NP_001351427.1:n.1531+44_1531+50del
NM_001364499.1:c.1531+44_1531+50del NP_001351428.1:n.1531+44_1531+50del
NM_001364500.1:c.1531+44_1531+50del NP_001351429.1:n.1531+44_1531+50del
NR_157195.1:n.2164+44_2164+50del
NR_157196.1:n.1868+40_1868+46del
XM_017011812.2:c.1090+44_1090+50del XP_016867301.1:n.1090+44_1090+50del
XR_928190.2:n.246+11437_246+11443del
NM_130797.4:c.1714+44_1714+50del MANE Select NP_570629.2:n.1714+44_1714+50del
NM_001039350.3:c.1522+44_1522+50del NP_001034439.1:n.1522+44_1522+50del
NM_001290252.2:c.1393+44_1393+50del NP_001277181.1:n.1393+44_1393+50del
NM_001364497.2:c.1531+44_1531+50del NP_001351426.1:n.1531+44_1531+50del
NM_001364498.2:c.1531+44_1531+50del NP_001351427.1:n.1531+44_1531+50del
NM_001364499.2:c.1531+44_1531+50del NP_001351428.1:n.1531+44_1531+50del
NM_001364500.2:c.1531+44_1531+50del NP_001351429.1:n.1531+44_1531+50del
NM_001936.5:c.1528+44_1528+50del NP_001927.3:n.1528+44_1528+50del
NR_157196.2:n.1868+40_1868+46del
NR_157195.2:n.2164+44_2164+50del