Canonical Allele Identifier: CA835523135

Gene: DPP6

Linked Data

• dbSNP Id: rs1407765479
• gnomAD v3: 7-153861609-T-G
• gnomAD v4: 7-153861609-T-G
• MyVariant Identifiers: chr7:g.153558694T>G (hg19) ; chr7:g.153861609T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.153861609T>G , CM000669.2:g.153861609T>G	GRCh38
NC_000007.13:g.153558694T>G , CM000669.1:g.153558694T>G	GRCh37
NC_000007.12:g.153189627T>G	NCBI36
NG_033878.2:g.118624T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.60+112601T>G	ENSP00000516215.1:n.60+112601T>G
NM_001364497.1:c.60+112601T>G	NP_001351426.1:n.60+112601T>G
NM_001364498.1:c.60+112601T>G	NP_001351427.1:n.60+112601T>G
NM_001364499.1:c.60+112601T>G	NP_001351428.1:n.60+112601T>G
NM_001364500.1:c.60+112601T>G	NP_001351429.1:n.60+112601T>G
XR_001745002.1:n.3345+2986T>G
NM_001364497.2:c.60+112601T>G	NP_001351426.1:n.60+112601T>G
NM_001364498.2:c.60+112601T>G	NP_001351427.1:n.60+112601T>G
NM_001364499.2:c.60+112601T>G	NP_001351428.1:n.60+112601T>G
NM_001364500.2:c.60+112601T>G	NP_001351429.1:n.60+112601T>G