Canonical Allele Identifier: CA169614024

Gene: DPP6

Linked Data

• dbSNP Id: rs562987059
• gnomAD v3: 7-153861832-C-G
• gnomAD v4: 7-153861832-C-G
• MyVariant Identifiers: chr7:g.153558917C>G (hg19) ; chr7:g.153861832C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.153861832C>G , CM000669.2:g.153861832C>G	GRCh38
NC_000007.13:g.153558917C>G , CM000669.1:g.153558917C>G	GRCh37
NC_000007.12:g.153189850C>G	NCBI36
NG_033878.2:g.118847C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706130.1:c.60+112824C>G	ENSP00000516215.1:n.60+112824C>G
NM_001364497.1:c.60+112824C>G	NP_001351426.1:n.60+112824C>G
NM_001364498.1:c.60+112824C>G	NP_001351427.1:n.60+112824C>G
NM_001364499.1:c.60+112824C>G	NP_001351428.1:n.60+112824C>G
NM_001364500.1:c.60+112824C>G	NP_001351429.1:n.60+112824C>G
XR_001745002.1:n.3346-3074C>G
NM_001364497.2:c.60+112824C>G	NP_001351426.1:n.60+112824C>G
NM_001364498.2:c.60+112824C>G	NP_001351427.1:n.60+112824C>G
NM_001364499.2:c.60+112824C>G	NP_001351428.1:n.60+112824C>G
NM_001364500.2:c.60+112824C>G	NP_001351429.1:n.60+112824C>G