Canonical Allele Identifier: CA370114912

Gene: DPP6

Linked Data

• MyVariant Identifiers: chr7:g.154645492C>G (hg19) ; chr7:g.154853782C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.154853782C>G , CM000669.2:g.154853782C>G	GRCh38
NC_000007.13:g.154645492C>G , CM000669.1:g.154645492C>G	GRCh37
NC_000007.12:g.154276425C>G	NCBI36
NG_033878.1:g.971449C>G
NG_033878.2:g.1110797C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.1486C>G	ENSP00000516215.1:p.Pro496Ala
ENST00000706151.1:c.694C>G	ENSP00000516234.1:p.Pro232Ala
ENST00000706153.1:n.1315C>G
ENST00000706154.1:n.953C>G
ENST00000706155.1:n.1100C>G
ENST00000377770.8:c.1669C>G MANE Select	ENSP00000367001.3:p.Pro557Ala
ENST00000332007.7:c.1483C>G	ENSP00000328226.3:p.Pro495Ala
ENST00000377770.7:c.1669C>G	ENSP00000367001.3:p.Pro557Ala
ENST00000404039.5:c.1477C>G	ENSP00000385578.1:p.Pro493Ala
ENST00000427557.1:c.1348C>G	ENSP00000397303.1:p.Pro450Ala
ENST00000493268.1:n.234C>G
NM_001039350.2:c.1477C>G	NP_001034439.1:p.Pro493Ala
NM_001290252.1:c.1348C>G	NP_001277181.1:p.Pro450Ala
NM_001936.4:c.1483C>G	NP_001927.3:p.Pro495Ala
NM_130797.3:c.1669C>G	NP_570629.2:p.Pro557Ala
XM_011515865.1:c.1477C>G	XP_011514167.1:p.Pro493Ala
XM_011515866.1:c.1045C>G	XP_011514168.1:p.Pro349Ala
XR_928190.1:n.154+11528G>C
NM_001364497.1:c.1486C>G	NP_001351426.1:p.Pro496Ala
NM_001364498.1:c.1486C>G	NP_001351427.1:p.Pro496Ala
NM_001364499.1:c.1486C>G	NP_001351428.1:p.Pro496Ala
NM_001364500.1:c.1486C>G	NP_001351429.1:p.Pro496Ala
NR_157195.1:n.2119C>G
NR_157196.1:n.1819C>G
XM_017011812.2:c.1045C>G	XP_016867301.1:p.Pro349Ala
XR_928190.2:n.246+11528G>C
NM_130797.4:c.1669C>G MANE Select	NP_570629.2:p.Pro557Ala
NM_001039350.3:c.1477C>G	NP_001034439.1:p.Pro493Ala
NM_001290252.2:c.1348C>G	NP_001277181.1:p.Pro450Ala
NM_001364497.2:c.1486C>G	NP_001351426.1:p.Pro496Ala
NM_001364498.2:c.1486C>G	NP_001351427.1:p.Pro496Ala
NM_001364499.2:c.1486C>G	NP_001351428.1:p.Pro496Ala
NM_001364500.2:c.1486C>G	NP_001351429.1:p.Pro496Ala
NM_001936.5:c.1483C>G	NP_001927.3:p.Pro495Ala
NR_157196.2:n.1819C>G
NR_157195.2:n.2119C>G