Canonical Allele Identifier: CA169614011

Gene: DPP6

Linked Data

• dbSNP Id: rs576198026
• gnomAD v2: 7-153558734-T-C
• gnomAD v3: 7-153861649-T-C
• gnomAD v4: 7-153861649-T-C
• MyVariant Identifiers: chr7:g.153558734T>C (hg19) ; chr7:g.153861649T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.153861649T>C , CM000669.2:g.153861649T>C	GRCh38
NC_000007.13:g.153558734T>C , CM000669.1:g.153558734T>C	GRCh37
NC_000007.12:g.153189667T>C	NCBI36
NG_033878.2:g.118664T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.60+112641T>C	ENSP00000516215.1:n.60+112641T>C
NM_001364497.1:c.60+112641T>C	NP_001351426.1:n.60+112641T>C
NM_001364498.1:c.60+112641T>C	NP_001351427.1:n.60+112641T>C
NM_001364499.1:c.60+112641T>C	NP_001351428.1:n.60+112641T>C
NM_001364500.1:c.60+112641T>C	NP_001351429.1:n.60+112641T>C
XR_001745002.1:n.3345+3026T>C
NM_001364497.2:c.60+112641T>C	NP_001351426.1:n.60+112641T>C
NM_001364498.2:c.60+112641T>C	NP_001351427.1:n.60+112641T>C
NM_001364499.2:c.60+112641T>C	NP_001351428.1:n.60+112641T>C
NM_001364500.2:c.60+112641T>C	NP_001351429.1:n.60+112641T>C