Canonical Allele Identifier: CA370204339
Community Standard Title: NM_130797.4(DPP6):c.1153A>G (p.Met385Val)
Gene: DPP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.154794095A>G , CM000669.2:g.154794095A>G GRCh38
NC_000007.13:g.154585805A>G , CM000669.1:g.154585805A>G GRCh37
NC_000007.12:g.154216738A>G NCBI36
NG_033878.1:g.911762A>G
NG_033878.2:g.1051110A>G

Transcript Alleles

HGVS Amino-acid Change
NM_130797.4:c.1153A>G MANE Select NP_570629.2:p.Met385Val
ENST00000377770.8:c.1153A>G MANE Select ENSP00000367001.3:p.Met385Val
NM_001039350.2:c.961A>G NP_001034439.1:p.Met321Val
NM_001039350.3:c.961A>G NP_001034439.1:p.Met321Val
NM_001290252.1:c.832A>G NP_001277181.1:p.Met278Val
NM_001290252.2:c.832A>G NP_001277181.1:p.Met278Val
NM_001364497.1:c.970A>G NP_001351426.1:p.Met324Val
NM_001364497.2:c.970A>G NP_001351426.1:p.Met324Val
NM_001364498.1:c.970A>G NP_001351427.1:p.Met324Val
NM_001364498.2:c.970A>G NP_001351427.1:p.Met324Val
NM_001364499.1:c.970A>G NP_001351428.1:p.Met324Val
NM_001364499.2:c.970A>G NP_001351428.1:p.Met324Val
NM_001364500.1:c.970A>G NP_001351429.1:p.Met324Val
NM_001364500.2:c.970A>G NP_001351429.1:p.Met324Val
NM_001364501.1:c.961A>G NP_001351430.1:p.Met321Val
NM_001364501.2:c.961A>G NP_001351430.1:p.Met321Val
NM_001936.4:c.967A>G NP_001927.3:p.Met323Val
NM_001936.5:c.967A>G NP_001927.3:p.Met323Val
NM_130797.3:c.1153A>G NP_570629.2:p.Met385Val
NR_157195.1:n.1603A>G
NR_157195.2:n.1603A>G
NR_157196.1:n.1303A>G
NR_157196.2:n.1303A>G
ENST00000332007.7:c.967A>G ENSP00000328226.3:p.Met323Val
ENST00000377770.7:c.1153A>G ENSP00000367001.3:p.Met385Val
ENST00000404039.5:c.961A>G ENSP00000385578.1:p.Met321Val
ENST00000427557.1:c.832A>G ENSP00000397303.1:p.Met278Val
ENST00000471100.5:n.299A>G
ENST00000478614.1:n.371A>G
ENST00000481593.1:n.172A>G
ENST00000706130.1:c.970A>G ENSP00000516215.1:p.Met324Val
ENST00000706151.1:c.178A>G ENSP00000516234.1:p.Met60Val
ENST00000706153.1:n.799A>G
ENST00000706154.1:n.437A>G
ENST00000706155.1:n.584A>G
XM_011515865.1:c.961A>G XP_011514167.1:p.Met321Val
XM_011515866.1:c.529A>G XP_011514168.1:p.Met177Val
XM_017011812.2:c.529A>G XP_016867301.1:p.Met177Val