Canonical Allele Identifier: CA458715746

Gene: DPP6

Linked Data

• MyVariant Identifiers: chr7:g.154645515G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.154853805G>C , CM000669.2:g.154853805G>C	GRCh38
NC_000007.13:g.154645515G>C , CM000669.1:g.154645515G>C	GRCh37
NC_000007.12:g.154276448G>C	NCBI36
NG_033878.1:g.971472G>C
NG_033878.2:g.1110820G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.1509G>C	ENSP00000516215.1:p.Val503=
ENST00000706151.1:c.717G>C	ENSP00000516234.1:p.Val239=
ENST00000706153.1:n.1338G>C
ENST00000706154.1:n.976G>C
ENST00000706155.1:n.1123G>C
ENST00000377770.8:c.1692G>C MANE Select	ENSP00000367001.3:p.Val564=
ENST00000332007.7:c.1506G>C	ENSP00000328226.3:p.Val502=
ENST00000377770.7:c.1692G>C	ENSP00000367001.3:p.Val564=
ENST00000404039.5:c.1500G>C	ENSP00000385578.1:p.Val500=
ENST00000427557.1:c.1371G>C	ENSP00000397303.1:p.Val457=
ENST00000493268.1:n.257G>C
NM_001039350.2:c.1500G>C	NP_001034439.1:p.Val500=
NM_001290252.1:c.1371G>C	NP_001277181.1:p.Val457=
NM_001936.4:c.1506G>C	NP_001927.3:p.Val502=
NM_130797.3:c.1692G>C	NP_570629.2:p.Val564=
XM_011515865.1:c.1500G>C	XP_011514167.1:p.Val500=
XM_011515866.1:c.1068G>C	XP_011514168.1:p.Val356=
XR_928190.1:n.154+11505C>G
NM_001364497.1:c.1509G>C	NP_001351426.1:p.Val503=
NM_001364498.1:c.1509G>C	NP_001351427.1:p.Val503=
NM_001364499.1:c.1509G>C	NP_001351428.1:p.Val503=
NM_001364500.1:c.1509G>C	NP_001351429.1:p.Val503=
NR_157195.1:n.2142G>C
NR_157196.1:n.1842G>C
XM_017011812.2:c.1068G>C	XP_016867301.1:p.Val356=
XR_928190.2:n.246+11505C>G
NM_130797.4:c.1692G>C MANE Select	NP_570629.2:p.Val564=
NM_001039350.3:c.1500G>C	NP_001034439.1:p.Val500=
NM_001290252.2:c.1371G>C	NP_001277181.1:p.Val457=
NM_001364497.2:c.1509G>C	NP_001351426.1:p.Val503=
NM_001364498.2:c.1509G>C	NP_001351427.1:p.Val503=
NM_001364499.2:c.1509G>C	NP_001351428.1:p.Val503=
NM_001364500.2:c.1509G>C	NP_001351429.1:p.Val503=
NM_001936.5:c.1506G>C	NP_001927.3:p.Val502=
NR_157196.2:n.1842G>C
NR_157195.2:n.2142G>C