Canonical Allele Identifier: CA381232618

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65348932G>A , CM000673.2:g.65348932G>A	GRCh38
NC_000011.9:g.65116403G>A , CM000673.1:g.65116403G>A	GRCh37
NC_000011.8:g.64872979G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006268.5:c.1099+1G>A MANE Select	NP_006259.1:n.1099+1G>A
ENST00000528416.6:c.1099+1G>A MANE Select	ENSP00000436901.1:n.1099+1G>A
NM_001330308.1:c.1141+1G>A	NP_001317237.1:n.1141+1G>A
NM_001330308.2:c.1141+1G>A	NP_001317237.1:n.1141+1G>A
NM_006268.4:c.1099+1G>A	NP_006259.1:n.1099+1G>A
ENST00000252268.8:c.1141+1G>A	ENSP00000252268.4:n.1141+1G>A
ENST00000415073.6:c.547+1G>A	ENSP00000399714.2:n.547+1G>A
ENST00000524666.5:n.3541+1G>A
ENST00000528416.5:c.1099+1G>A	ENSP00000436901.1:n.1099+1G>A
ENST00000530993.6:c.163+1G>A	ENSP00000515294.1:n.163+1G>A
ENST00000531989.1:c.274+1G>A	ENSP00000435887.1:n.274+1G>A
ENST00000532052.1:n.1868+1G>A
ENST00000703393.1:c.*83+1G>A	ENSP00000515285.1:n.*83+1G>A
ENST00000703394.1:n.1311+1G>A
ENST00000703424.1:c.1651+1G>A	ENSP00000515295.1:n.1651+1G>A
ENST00000703425.1:c.1210+1G>A	ENSP00000515296.1:n.1210+1G>A
ENST00000703426.1:c.*996+1G>A	ENSP00000515297.1:n.*996+1G>A
ENST00000703427.1:c.1039+1G>A	ENSP00000515298.1:n.1039+1G>A
XM_005274149.1:c.1141+1G>A	XP_005274206.1:n.1141+1G>A
XM_017018101.2:c.1081+1G>A	XP_016873590.1:n.1081+1G>A
XM_017018102.1:c.1039+1G>A	XP_016873591.1:n.1039+1G>A
XM_024448637.1:c.1651+1G>A	XP_024304405.1:n.1651+1G>A
XM_024448638.1:c.1591+1G>A	XP_024304406.1:n.1591+1G>A
XR_950008.1:n.1067+1G>A
XR_950008.3:n.1067+1G>A