Canonical Allele Identifier: CA169614003

Gene: DPP6

Linked Data

• dbSNP Id: rs768229977
• gnomAD v2: 7-153558680-C-CT
• gnomAD v3: 7-153861595-C-CT
• gnomAD v4: 7-153861595-C-CT
• COSMIC: COSN23620227
• MyVariant Identifiers: chr7:g.153558680_153558681insT (hg19) ; chr7:g.153861595_153861596insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.153861601dup , CM000669.2:g.153861601dup	GRCh38
NC_000007.13:g.153558686dup , CM000669.1:g.153558686dup	GRCh37
NC_000007.12:g.153189619dup	NCBI36
NG_033878.2:g.118616dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.60+112593dup	ENSP00000516215.1:n.60+112593dup
NM_001364497.1:c.60+112593dup	NP_001351426.1:n.60+112593dup
NM_001364498.1:c.60+112593dup	NP_001351427.1:n.60+112593dup
NM_001364499.1:c.60+112593dup	NP_001351428.1:n.60+112593dup
NM_001364500.1:c.60+112593dup	NP_001351429.1:n.60+112593dup
XR_001745002.1:n.3345+2978dup
NM_001364497.2:c.60+112593dup	NP_001351426.1:n.60+112593dup
NM_001364498.2:c.60+112593dup	NP_001351427.1:n.60+112593dup
NM_001364499.2:c.60+112593dup	NP_001351428.1:n.60+112593dup
NM_001364500.2:c.60+112593dup	NP_001351429.1:n.60+112593dup