Canonical Allele Identifier: CA4583650

Gene: DPP6

Linked Data

• dbSNP Id: rs761312315
• ExAC: 7:154645516 C / T
• gnomAD v4: 7-154853806-C-T
• MyVariant Identifiers: chr7:g.154645516C>T (hg19) ; chr7:g.154853806C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.154853806C>T , CM000669.2:g.154853806C>T	GRCh38
NC_000007.13:g.154645516C>T , CM000669.1:g.154645516C>T	GRCh37
NC_000007.12:g.154276449C>T	NCBI36
NG_033878.1:g.971473C>T
NG_033878.2:g.1110821C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.1510C>T	ENSP00000516215.1:p.His504Tyr
ENST00000706151.1:c.718C>T	ENSP00000516234.1:p.His240Tyr
ENST00000706153.1:n.1339C>T
ENST00000706154.1:n.977C>T
ENST00000706155.1:n.1124C>T
ENST00000377770.8:c.1693C>T MANE Select	ENSP00000367001.3:p.His565Tyr
ENST00000332007.7:c.1507C>T	ENSP00000328226.3:p.His503Tyr
ENST00000377770.7:c.1693C>T	ENSP00000367001.3:p.His565Tyr
ENST00000404039.5:c.1501C>T	ENSP00000385578.1:p.His501Tyr
ENST00000427557.1:c.1372C>T	ENSP00000397303.1:p.His458Tyr
ENST00000493268.1:n.258C>T
NM_001039350.2:c.1501C>T	NP_001034439.1:p.His501Tyr
NM_001290252.1:c.1372C>T	NP_001277181.1:p.His458Tyr
NM_001936.4:c.1507C>T	NP_001927.3:p.His503Tyr
NM_130797.3:c.1693C>T	NP_570629.2:p.His565Tyr
XM_011515865.1:c.1501C>T	XP_011514167.1:p.His501Tyr
XM_011515866.1:c.1069C>T	XP_011514168.1:p.His357Tyr
XR_928190.1:n.154+11504G>A
NM_001364497.1:c.1510C>T	NP_001351426.1:p.His504Tyr
NM_001364498.1:c.1510C>T	NP_001351427.1:p.His504Tyr
NM_001364499.1:c.1510C>T	NP_001351428.1:p.His504Tyr
NM_001364500.1:c.1510C>T	NP_001351429.1:p.His504Tyr
NR_157195.1:n.2143C>T
NR_157196.1:n.1843C>T
XM_017011812.2:c.1069C>T	XP_016867301.1:p.His357Tyr
XR_928190.2:n.246+11504G>A
NM_130797.4:c.1693C>T MANE Select	NP_570629.2:p.His565Tyr
NM_001039350.3:c.1501C>T	NP_001034439.1:p.His501Tyr
NM_001290252.2:c.1372C>T	NP_001277181.1:p.His458Tyr
NM_001364497.2:c.1510C>T	NP_001351426.1:p.His504Tyr
NM_001364498.2:c.1510C>T	NP_001351427.1:p.His504Tyr
NM_001364499.2:c.1510C>T	NP_001351428.1:p.His504Tyr
NM_001364500.2:c.1510C>T	NP_001351429.1:p.His504Tyr
NM_001936.5:c.1507C>T	NP_001927.3:p.His503Tyr
NR_157196.2:n.1843C>T
NR_157195.2:n.2143C>T