Canonical Allele Identifier: CA1753874124

Gene: DPP6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.153934563G= , CM000669.2:g.153934563G=	GRCh38
NC_000007.13:g.153631648G= , CM000669.1:g.153631648G=	GRCh37
NC_000007.12:g.153262581G=	NCBI36
NG_033878.1:g.52230G=
NG_033878.2:g.191578G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001039350.2:c.51+46829G=	NP_001034439.1:n.51+46829G=
NM_001039350.3:c.51+46829G=	NP_001034439.1:n.51+46829G=
NM_001364497.1:c.60+185555G=	NP_001351426.1:n.60+185555G=
NM_001364497.2:c.60+185555G=	NP_001351426.1:n.60+185555G=
NM_001364498.1:c.60+185555G=	NP_001351427.1:n.60+185555G=
NM_001364498.2:c.60+185555G=	NP_001351427.1:n.60+185555G=
NM_001364499.1:c.60+185555G=	NP_001351428.1:n.60+185555G=
NM_001364499.2:c.60+185555G=	NP_001351428.1:n.60+185555G=
NM_001364500.1:c.60+185555G=	NP_001351429.1:n.60+185555G=
NM_001364500.2:c.60+185555G=	NP_001351429.1:n.60+185555G=
NM_001364501.1:c.51+46829G=	NP_001351430.1:n.51+46829G=
NM_001364501.2:c.51+46829G=	NP_001351430.1:n.51+46829G=
NR_157195.1:n.693+46829G=
NR_157195.2:n.693+46829G=
ENST00000404039.5:c.51+46829G=	ENSP00000385578.1:n.51+46829G=
ENST00000706130.1:c.60+185555G=	ENSP00000516215.1:n.60+185555G=
XM_011515865.1:c.51+46829G=	XP_011514167.1:n.51+46829G=