Canonical Allele Identifier: CA3188108112

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65346072T= , CM000673.2:g.65346072T=	GRCh38
NC_000011.9:g.65113543T= , CM000673.1:g.65113543T=	GRCh37
NC_000011.8:g.64870119T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006268.5:c.904+14T= MANE Select	NP_006259.1:n.904+14T=
ENST00000528416.6:c.904+14T= MANE Select	ENSP00000436901.1:n.904+14T=
NM_001330308.1:c.946+14T=	NP_001317237.1:n.946+14T=
NM_001330308.2:c.946+14T=	NP_001317237.1:n.946+14T=
NM_006268.4:c.904+14T=	NP_006259.1:n.904+14T=
ENST00000252268.8:c.946+14T=	ENSP00000252268.4:n.946+14T=
ENST00000415073.6:c.466-2778T=	ENSP00000399714.2:n.466-2778T=
ENST00000524666.5:n.682T=
ENST00000528416.5:c.904+14T=	ENSP00000436901.1:n.904+14T=
ENST00000530973.1:n.655T=
ENST00000530993.6:c.-33+14T=	ENSP00000515294.1:n.-33+14T=
ENST00000531989.1:c.192+14T=	ENSP00000435887.1:n.192+14T=
ENST00000532052.1:n.1673+14T=
ENST00000703393.1:c.904+14T=	ENSP00000515285.1:n.904+14T=
ENST00000703394.1:n.1116+14T=
ENST00000703424.1:c.1456+14T=	ENSP00000515295.1:n.1456+14T=
ENST00000703425.1:c.1015+14T=	ENSP00000515296.1:n.1015+14T=
ENST00000703426.1:c.*801+14T=	ENSP00000515297.1:n.*801+14T=
ENST00000703427.1:c.844+14T=	ENSP00000515298.1:n.844+14T=
XM_005274149.1:c.946+14T=	XP_005274206.1:n.946+14T=
XM_017018101.2:c.886+14T=	XP_016873590.1:n.886+14T=
XM_017018102.1:c.844+14T=	XP_016873591.1:n.844+14T=
XM_024448637.1:c.1456+14T=	XP_024304405.1:n.1456+14T=
XM_024448638.1:c.1396+14T=	XP_024304406.1:n.1396+14T=
XR_950008.1:n.872+14T=
XR_950008.3:n.872+14T=