Canonical Allele Identifier: CA1754324584

Gene: DPP6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.154853892_154853894delinsTGA , CM000669.2:g.154853892_154853894delinsTGA	GRCh38
NC_000007.13:g.154645602_154645604delinsTGA , CM000669.1:g.154645602_154645604delinsTGA	GRCh37
NC_000007.12:g.154276535_154276537delinsTGA	NCBI36
NG_033878.1:g.971559_971561delinsTGA
NG_033878.2:g.1110907_1110909delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.1531+65_1531+67delinsTGA	ENSP00000516215.1:n.1531+65_1531+67delinsTGA
ENST00000706151.1:c.739+65_739+67delinsTGA	ENSP00000516234.1:n.739+65_739+67delinsTGA
ENST00000706153.1:n.1360+65_1360+67delinsTGA
ENST00000706154.1:n.998+65_998+67delinsTGA
ENST00000706155.1:n.1145+65_1145+67delinsTGA
ENST00000377770.8:c.1714+65_1714+67delinsTGA MANE Select	ENSP00000367001.3:n.1714+65_1714+67delinsTGA
ENST00000332007.7:c.1528+65_1528+67delinsTGA	ENSP00000328226.3:n.1528+65_1528+67delinsTGA
ENST00000377770.7:c.1714+65_1714+67delinsTGA	ENSP00000367001.3:n.1714+65_1714+67delinsTGA
ENST00000404039.5:c.1522+65_1522+67delinsTGA	ENSP00000385578.1:n.1522+65_1522+67delinsTGA
ENST00000427557.1:c.1393+65_1393+67delinsTGA	ENSP00000397303.1:n.1393+65_1393+67delinsTGA
ENST00000493268.1:n.279+65_279+67delinsTGA
NM_001039350.2:c.1522+65_1522+67delinsTGA	NP_001034439.1:n.1522+65_1522+67delinsTGA
NM_001290252.1:c.1393+65_1393+67delinsTGA	NP_001277181.1:n.1393+65_1393+67delinsTGA
NM_001936.4:c.1528+65_1528+67delinsTGA	NP_001927.3:n.1528+65_1528+67delinsTGA
NM_130797.3:c.1714+65_1714+67delinsTGA	NP_570629.2:n.1714+65_1714+67delinsTGA
XM_011515865.1:c.1522+65_1522+67delinsTGA	XP_011514167.1:n.1522+65_1522+67delinsTGA
XM_011515866.1:c.1090+65_1090+67delinsTGA	XP_011514168.1:n.1090+65_1090+67delinsTGA
XR_928190.1:n.154+11416_154+11418delinsTCA
NM_001364497.1:c.1531+65_1531+67delinsTGA	NP_001351426.1:n.1531+65_1531+67delinsTGA
NM_001364498.1:c.1531+65_1531+67delinsTGA	NP_001351427.1:n.1531+65_1531+67delinsTGA
NM_001364499.1:c.1531+65_1531+67delinsTGA	NP_001351428.1:n.1531+65_1531+67delinsTGA
NM_001364500.1:c.1531+65_1531+67delinsTGA	NP_001351429.1:n.1531+65_1531+67delinsTGA
NR_157195.1:n.2164+65_2164+67delinsTGA
NR_157196.1:n.1868+61_1868+63delinsTGA
XM_017011812.2:c.1090+65_1090+67delinsTGA	XP_016867301.1:n.1090+65_1090+67delinsTGA
XR_928190.2:n.246+11416_246+11418delinsTCA
NM_130797.4:c.1714+65_1714+67delinsTGA MANE Select	NP_570629.2:n.1714+65_1714+67delinsTGA
NM_001039350.3:c.1522+65_1522+67delinsTGA	NP_001034439.1:n.1522+65_1522+67delinsTGA
NM_001290252.2:c.1393+65_1393+67delinsTGA	NP_001277181.1:n.1393+65_1393+67delinsTGA
NM_001364497.2:c.1531+65_1531+67delinsTGA	NP_001351426.1:n.1531+65_1531+67delinsTGA
NM_001364498.2:c.1531+65_1531+67delinsTGA	NP_001351427.1:n.1531+65_1531+67delinsTGA
NM_001364499.2:c.1531+65_1531+67delinsTGA	NP_001351428.1:n.1531+65_1531+67delinsTGA
NM_001364500.2:c.1531+65_1531+67delinsTGA	NP_001351429.1:n.1531+65_1531+67delinsTGA
NM_001936.5:c.1528+65_1528+67delinsTGA	NP_001927.3:n.1528+65_1528+67delinsTGA
NR_157196.2:n.1868+61_1868+63delinsTGA
NR_157195.2:n.2164+65_2164+67delinsTGA