Canonical Allele Identifier: CA4583406

Gene: DPP6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.154772897C>G , CM000669.2:g.154772897C>G	GRCh38
NC_000007.13:g.154564607C>G , CM000669.1:g.154564607C>G	GRCh37
NC_000007.12:g.154195540C>G	NCBI36
NG_033878.1:g.890564C>G
NG_033878.2:g.1029912C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_130797.4:c.1091C>G MANE Select	NP_570629.2:p.Pro364Arg
ENST00000377770.8:c.1091C>G MANE Select	ENSP00000367001.3:p.Pro364Arg
NM_001039350.2:c.899C>G	NP_001034439.1:p.Pro300Arg
NM_001039350.3:c.899C>G	NP_001034439.1:p.Pro300Arg
NM_001290252.1:c.770C>G	NP_001277181.1:p.Pro257Arg
NM_001290252.2:c.770C>G	NP_001277181.1:p.Pro257Arg
NM_001364497.1:c.908C>G	NP_001351426.1:p.Pro303Arg
NM_001364497.2:c.908C>G	NP_001351426.1:p.Pro303Arg
NM_001364498.1:c.908C>G	NP_001351427.1:p.Pro303Arg
NM_001364498.2:c.908C>G	NP_001351427.1:p.Pro303Arg
NM_001364499.1:c.908C>G	NP_001351428.1:p.Pro303Arg
NM_001364499.2:c.908C>G	NP_001351428.1:p.Pro303Arg
NM_001364500.1:c.908C>G	NP_001351429.1:p.Pro303Arg
NM_001364500.2:c.908C>G	NP_001351429.1:p.Pro303Arg
NM_001364501.1:c.899C>G	NP_001351430.1:p.Pro300Arg
NM_001364501.2:c.899C>G	NP_001351430.1:p.Pro300Arg
NM_001936.4:c.905C>G	NP_001927.3:p.Pro302Arg
NM_001936.5:c.905C>G	NP_001927.3:p.Pro302Arg
NM_130797.3:c.1091C>G	NP_570629.2:p.Pro364Arg
NR_157195.1:n.1541C>G
NR_157195.2:n.1541C>G
NR_157196.1:n.1241C>G
NR_157196.2:n.1241C>G
ENST00000332007.7:c.905C>G	ENSP00000328226.3:p.Pro302Arg
ENST00000377770.7:c.1091C>G	ENSP00000367001.3:p.Pro364Arg
ENST00000404039.5:c.899C>G	ENSP00000385578.1:p.Pro300Arg
ENST00000427557.1:c.770C>G	ENSP00000397303.1:p.Pro257Arg
ENST00000706130.1:c.908C>G	ENSP00000516215.1:p.Pro303Arg
ENST00000706151.1:c.116C>G	ENSP00000516234.1:p.Pro39Arg
ENST00000706153.1:n.737C>G
ENST00000706154.1:n.375C>G
ENST00000706155.1:n.522C>G
ENST00000706156.1:n.14C>G
XM_011515865.1:c.899C>G	XP_011514167.1:p.Pro300Arg
XM_011515866.1:c.467C>G	XP_011514168.1:p.Pro156Arg
XM_017011812.2:c.467C>G	XP_016867301.1:p.Pro156Arg