Canonical Allele Identifier: CA169614032

Gene: DPP6

Linked Data

• dbSNP Id: rs12671878
• gnomAD v2: 7-153558949-C-T
• gnomAD v3: 7-153861864-C-T
• gnomAD v4: 7-153861864-C-T
• MyVariant Identifiers: chr7:g.153558949C>T (hg19) ; chr7:g.153861864C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.153861864C>T , CM000669.2:g.153861864C>T	GRCh38
NC_000007.13:g.153558949C>T , CM000669.1:g.153558949C>T	GRCh37
NC_000007.12:g.153189882C>T	NCBI36
NG_033878.2:g.118879C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706130.1:c.60+112856C>T	ENSP00000516215.1:n.60+112856C>T
NM_001364497.1:c.60+112856C>T	NP_001351426.1:n.60+112856C>T
NM_001364498.1:c.60+112856C>T	NP_001351427.1:n.60+112856C>T
NM_001364499.1:c.60+112856C>T	NP_001351428.1:n.60+112856C>T
NM_001364500.1:c.60+112856C>T	NP_001351429.1:n.60+112856C>T
XR_001745002.1:n.3346-3042C>T
NM_001364497.2:c.60+112856C>T	NP_001351426.1:n.60+112856C>T
NM_001364498.2:c.60+112856C>T	NP_001351427.1:n.60+112856C>T
NM_001364499.2:c.60+112856C>T	NP_001351428.1:n.60+112856C>T
NM_001364500.2:c.60+112856C>T	NP_001351429.1:n.60+112856C>T