Canonical Allele Identifier: CA381254347

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65346011C>T , CM000673.2:g.65346011C>T	GRCh38
NC_000011.9:g.65113482C>T , CM000673.1:g.65113482C>T	GRCh37
NC_000011.8:g.64870058C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006268.5:c.857C>T MANE Select	NP_006259.1:p.Thr286Met
ENST00000528416.6:c.857C>T MANE Select	ENSP00000436901.1:p.Thr286Met
NM_001330308.1:c.899C>T	NP_001317237.1:p.Thr300Met
NM_001330308.2:c.899C>T	NP_001317237.1:p.Thr300Met
NM_006268.4:c.857C>T	NP_006259.1:p.Thr286Met
ENST00000252268.8:c.899C>T	ENSP00000252268.4:p.Thr300Met
ENST00000415073.6:c.466-2839C>T	ENSP00000399714.2:n.466-2839C>T
ENST00000524666.5:n.621C>T
ENST00000528416.5:c.857C>T	ENSP00000436901.1:p.Thr286Met
ENST00000530973.1:n.594C>T
ENST00000530993.6:c.-80C>T	ENSP00000515294.1:n.-80C>T
ENST00000531989.1:c.145C>T	ENSP00000435887.1:p.Arg49Trp
ENST00000532052.1:n.1626C>T
ENST00000532264.5:n.708C>T
ENST00000703393.1:c.857C>T	ENSP00000515285.1:p.Thr286Met
ENST00000703394.1:n.1069C>T
ENST00000703424.1:c.1409C>T	ENSP00000515295.1:p.Thr470Met
ENST00000703425.1:c.968C>T	ENSP00000515296.1:p.Thr323Met
ENST00000703426.1:c.*754C>T	ENSP00000515297.1:n.*754C>T
ENST00000703427.1:c.797C>T	ENSP00000515298.1:p.Thr266Met
XM_005274149.1:c.899C>T	XP_005274206.1:p.Thr300Met
XM_017018101.2:c.839C>T	XP_016873590.1:p.Thr280Met
XM_017018102.1:c.797C>T	XP_016873591.1:p.Thr266Met
XM_024448637.1:c.1409C>T	XP_024304405.1:p.Thr470Met
XM_024448638.1:c.1349C>T	XP_024304406.1:p.Thr450Met
XR_950008.1:n.825C>T
XR_950008.3:n.825C>T