Canonical Allele Identifier: CA223956448

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65343998G>T , CM000673.2:g.65343998G>T	GRCh38
NC_000011.9:g.65111469G>T , CM000673.1:g.65111469G>T	GRCh37
NC_000011.8:g.64868045G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530993.6:c.-413G>T	ENSP00000515294.1:n.-413G>T
ENST00000703393.1:c.566G>T	ENSP00000515285.1:p.Gly189Val
ENST00000703394.1:n.610G>T
ENST00000703424.1:c.566G>T	ENSP00000515295.1:p.Gly189Val
ENST00000703425.1:c.635G>T	ENSP00000515296.1:p.Gly212Val
ENST00000703426.1:c.*421G>T	ENSP00000515297.1:n.*421G>T
ENST00000703427.1:c.506G>T	ENSP00000515298.1:p.Gly169Val
ENST00000528416.6:c.566G>T MANE Select	ENSP00000436901.1:p.Gly189Val
ENST00000252268.8:c.566G>T	ENSP00000252268.4:p.Gly189Val
ENST00000415073.6:c.465+2436G>T	ENSP00000399714.2:n.465+2436G>T
ENST00000524666.5:n.401+161G>T
ENST00000528416.5:c.566G>T	ENSP00000436901.1:p.Gly189Val
ENST00000530973.1:n.177G>T
ENST00000530993.5:n.430G>T
ENST00000532102.5:c.*81G>T	ENSP00000434885.1:n.*81G>T
ENST00000532264.5:n.417G>T
ENST00000532492.1:n.341G>T
NM_006268.4:c.566G>T	NP_006259.1:p.Gly189Val
XM_005274149.1:c.566G>T	XP_005274206.1:p.Gly189Val
XR_950008.1:n.605+161G>T
NM_001330308.1:c.566G>T	NP_001317237.1:p.Gly189Val
XM_017018101.2:c.506G>T	XP_016873590.1:p.Gly169Val
XM_017018102.1:c.506G>T	XP_016873591.1:p.Gly169Val
XM_024448637.1:c.566G>T	XP_024304405.1:p.Gly189Val
XM_024448638.1:c.506G>T	XP_024304406.1:p.Gly169Val
XR_950008.3:n.605+161G>T
NM_006268.5:c.566G>T MANE Select	NP_006259.1:p.Gly189Val
NM_001330308.2:c.566G>T	NP_001317237.1:p.Gly189Val