Canonical Allele Identifier: CA370114952

Gene: DPP6

Linked Data

• dbSNP Id: rs1166705741
• gnomAD v2: 7-154645505-T-C
• gnomAD v4: 7-154853795-T-C
• MyVariant Identifiers: chr7:g.154645505T>C (hg19) ; chr7:g.154853795T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.154853795T>C , CM000669.2:g.154853795T>C	GRCh38
NC_000007.13:g.154645505T>C , CM000669.1:g.154645505T>C	GRCh37
NC_000007.12:g.154276438T>C	NCBI36
NG_033878.1:g.971462T>C
NG_033878.2:g.1110810T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706130.1:c.1499T>C	ENSP00000516215.1:p.Met500Thr
ENST00000706151.1:c.707T>C	ENSP00000516234.1:p.Met236Thr
ENST00000706153.1:n.1328T>C
ENST00000706154.1:n.966T>C
ENST00000706155.1:n.1113T>C
ENST00000377770.8:c.1682T>C MANE Select	ENSP00000367001.3:p.Met561Thr
ENST00000332007.7:c.1496T>C	ENSP00000328226.3:p.Met499Thr
ENST00000377770.7:c.1682T>C	ENSP00000367001.3:p.Met561Thr
ENST00000404039.5:c.1490T>C	ENSP00000385578.1:p.Met497Thr
ENST00000427557.1:c.1361T>C	ENSP00000397303.1:p.Met454Thr
ENST00000493268.1:n.247T>C
NM_001039350.2:c.1490T>C	NP_001034439.1:p.Met497Thr
NM_001290252.1:c.1361T>C	NP_001277181.1:p.Met454Thr
NM_001936.4:c.1496T>C	NP_001927.3:p.Met499Thr
NM_130797.3:c.1682T>C	NP_570629.2:p.Met561Thr
XM_011515865.1:c.1490T>C	XP_011514167.1:p.Met497Thr
XM_011515866.1:c.1058T>C	XP_011514168.1:p.Met353Thr
XR_928190.1:n.154+11515A>G
NM_001364497.1:c.1499T>C	NP_001351426.1:p.Met500Thr
NM_001364498.1:c.1499T>C	NP_001351427.1:p.Met500Thr
NM_001364499.1:c.1499T>C	NP_001351428.1:p.Met500Thr
NM_001364500.1:c.1499T>C	NP_001351429.1:p.Met500Thr
NR_157195.1:n.2132T>C
NR_157196.1:n.1832T>C
XM_017011812.2:c.1058T>C	XP_016867301.1:p.Met353Thr
XR_928190.2:n.246+11515A>G
NM_130797.4:c.1682T>C MANE Select	NP_570629.2:p.Met561Thr
NM_001039350.3:c.1490T>C	NP_001034439.1:p.Met497Thr
NM_001290252.2:c.1361T>C	NP_001277181.1:p.Met454Thr
NM_001364497.2:c.1499T>C	NP_001351426.1:p.Met500Thr
NM_001364498.2:c.1499T>C	NP_001351427.1:p.Met500Thr
NM_001364499.2:c.1499T>C	NP_001351428.1:p.Met500Thr
NM_001364500.2:c.1499T>C	NP_001351429.1:p.Met500Thr
NM_001936.5:c.1496T>C	NP_001927.3:p.Met499Thr
NR_157196.2:n.1832T>C
NR_157195.2:n.2132T>C