Canonical Allele Identifier: CA1754324529

Gene: DPP6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.154853801C= , CM000669.2:g.154853801C=	GRCh38
NC_000007.13:g.154645511C= , CM000669.1:g.154645511C=	GRCh37
NC_000007.12:g.154276444C=	NCBI36
NG_033878.1:g.971468C=
NG_033878.2:g.1110816C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.1505C=	ENSP00000516215.1:p.Thr502=
ENST00000706151.1:c.713C=	ENSP00000516234.1:p.Thr238=
ENST00000706153.1:n.1334C=
ENST00000706154.1:n.972C=
ENST00000706155.1:n.1119C=
ENST00000377770.8:c.1688C= MANE Select	ENSP00000367001.3:p.Thr563=
ENST00000332007.7:c.1502C=	ENSP00000328226.3:p.Thr501=
ENST00000377770.7:c.1688C=	ENSP00000367001.3:p.Thr563=
ENST00000404039.5:c.1496C=	ENSP00000385578.1:p.Thr499=
ENST00000427557.1:c.1367C=	ENSP00000397303.1:p.Thr456=
ENST00000493268.1:n.253C=
NM_001039350.2:c.1496C=	NP_001034439.1:p.Thr499=
NM_001290252.1:c.1367C=	NP_001277181.1:p.Thr456=
NM_001936.4:c.1502C=	NP_001927.3:p.Thr501=
NM_130797.3:c.1688C=	NP_570629.2:p.Thr563=
XM_011515865.1:c.1496C=	XP_011514167.1:p.Thr499=
XM_011515866.1:c.1064C=	XP_011514168.1:p.Thr355=
XR_928190.1:n.154+11509G=
NM_001364497.1:c.1505C=	NP_001351426.1:p.Thr502=
NM_001364498.1:c.1505C=	NP_001351427.1:p.Thr502=
NM_001364499.1:c.1505C=	NP_001351428.1:p.Thr502=
NM_001364500.1:c.1505C=	NP_001351429.1:p.Thr502=
NR_157195.1:n.2138C=
NR_157196.1:n.1838C=
XM_017011812.2:c.1064C=	XP_016867301.1:p.Thr355=
XR_928190.2:n.246+11509G=
NM_130797.4:c.1688C= MANE Select	NP_570629.2:p.Thr563=
NM_001039350.3:c.1496C=	NP_001034439.1:p.Thr499=
NM_001290252.2:c.1367C=	NP_001277181.1:p.Thr456=
NM_001364497.2:c.1505C=	NP_001351426.1:p.Thr502=
NM_001364498.2:c.1505C=	NP_001351427.1:p.Thr502=
NM_001364499.2:c.1505C=	NP_001351428.1:p.Thr502=
NM_001364500.2:c.1505C=	NP_001351429.1:p.Thr502=
NM_001936.5:c.1502C=	NP_001927.3:p.Thr501=
NR_157196.2:n.1838C=
NR_157195.2:n.2138C=