Canonical Allele Identifier: CA6095215

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65341020G>A , CM000673.2:g.65341020G>A	GRCh38
NC_000011.9:g.65108491G>A , CM000673.1:g.65108491G>A	GRCh37
NC_000011.8:g.64865067G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530993.6:c.-731G>A	ENSP00000515294.1:n.-731G>A
ENST00000703393.1:c.248G>A	ENSP00000515285.1:p.Arg83Gln
ENST00000703394.1:n.292G>A
ENST00000703424.1:c.248G>A	ENSP00000515295.1:p.Arg83Gln
ENST00000703425.1:c.317G>A	ENSP00000515296.1:p.Arg106Gln
ENST00000703426.1:c.*103G>A	ENSP00000515297.1:n.*103G>A
ENST00000703427.1:c.188G>A	ENSP00000515298.1:p.Arg63Gln
ENST00000528416.6:c.248G>A MANE Select	ENSP00000436901.1:p.Arg83Gln
ENST00000252268.8:c.248G>A	ENSP00000252268.4:p.Arg83Gln
ENST00000415073.6:c.248G>A	ENSP00000399714.2:p.Arg83Gln
ENST00000444314.6:n.283G>A
ENST00000524666.5:n.101G>A
ENST00000528416.5:c.248G>A	ENSP00000436901.1:p.Arg83Gln
ENST00000530993.5:n.112G>A
ENST00000532102.5:c.248G>A	ENSP00000434885.1:p.Arg83Gln
ENST00000532264.5:n.99G>A
NM_006268.4:c.248G>A	NP_006259.1:p.Arg83Gln
XM_005274149.1:c.248G>A	XP_005274206.1:p.Arg83Gln
XR_950008.1:n.295G>A
NM_001330308.1:c.248G>A	NP_001317237.1:p.Arg83Gln
XM_017018101.2:c.188G>A	XP_016873590.1:p.Arg63Gln
XM_017018102.1:c.188G>A	XP_016873591.1:p.Arg63Gln
XM_024448637.1:c.248G>A	XP_024304405.1:p.Arg83Gln
XM_024448638.1:c.188G>A	XP_024304406.1:p.Arg63Gln
XR_950008.3:n.295G>A
NM_006268.5:c.248G>A MANE Select	NP_006259.1:p.Arg83Gln
NM_001330308.2:c.248G>A	NP_001317237.1:p.Arg83Gln