Canonical Allele Identifier: CA381254308

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65345998A>T , CM000673.2:g.65345998A>T	GRCh38
NC_000011.9:g.65113469A>T , CM000673.1:g.65113469A>T	GRCh37
NC_000011.8:g.64870045A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006268.5:c.844A>T MANE Select	NP_006259.1:p.Ile282Phe
ENST00000528416.6:c.844A>T MANE Select	ENSP00000436901.1:p.Ile282Phe
NM_001330308.1:c.886A>T	NP_001317237.1:p.Ile296Phe
NM_001330308.2:c.886A>T	NP_001317237.1:p.Ile296Phe
NM_006268.4:c.844A>T	NP_006259.1:p.Ile282Phe
ENST00000252268.8:c.886A>T	ENSP00000252268.4:p.Ile296Phe
ENST00000415073.6:c.466-2852A>T	ENSP00000399714.2:n.466-2852A>T
ENST00000524666.5:n.608A>T
ENST00000528416.5:c.844A>T	ENSP00000436901.1:p.Ile282Phe
ENST00000530973.1:n.581A>T
ENST00000530993.6:c.-93A>T	ENSP00000515294.1:n.-93A>T
ENST00000531989.1:c.132A>T	ENSP00000435887.1:p.Arg44Ser
ENST00000532052.1:n.1613A>T
ENST00000532264.5:n.695A>T
ENST00000703393.1:c.844A>T	ENSP00000515285.1:p.Ile282Phe
ENST00000703394.1:n.1056A>T
ENST00000703424.1:c.1396A>T	ENSP00000515295.1:p.Ile466Phe
ENST00000703425.1:c.955A>T	ENSP00000515296.1:p.Ile319Phe
ENST00000703426.1:c.*741A>T	ENSP00000515297.1:n.*741A>T
ENST00000703427.1:c.784A>T	ENSP00000515298.1:p.Ile262Phe
XM_005274149.1:c.886A>T	XP_005274206.1:p.Ile296Phe
XM_017018101.2:c.826A>T	XP_016873590.1:p.Ile276Phe
XM_017018102.1:c.784A>T	XP_016873591.1:p.Ile262Phe
XM_024448637.1:c.1396A>T	XP_024304405.1:p.Ile466Phe
XM_024448638.1:c.1336A>T	XP_024304406.1:p.Ile446Phe
XR_950008.1:n.812A>T
XR_950008.3:n.812A>T