Canonical Allele Identifier: CA6095129

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65333907T>C , CM000673.2:g.65333907T>C	GRCh38
NC_000011.9:g.65101378T>C , CM000673.1:g.65101378T>C	GRCh37
NC_000011.8:g.64857954T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530993.6:c.-797T>C	ENSP00000515294.1:n.-797T>C
ENST00000703393.1:c.21T>C	ENSP00000515285.1:p.Asn7=
ENST00000703394.1:n.65T>C
ENST00000703424.1:c.21T>C	ENSP00000515295.1:p.Asn7=
ENST00000703425.1:c.21T>C	ENSP00000515296.1:p.Asn7=
ENST00000703426.1:c.21T>C	ENSP00000515297.1:p.Asn7=
ENST00000703427.1:c.-159T>C	ENSP00000515298.1:n.-159T>C
ENST00000528416.6:c.21T>C MANE Select	ENSP00000436901.1:p.Asn7=
ENST00000252268.8:c.21T>C	ENSP00000252268.4:p.Asn7=
ENST00000415073.6:c.21T>C	ENSP00000399714.2:p.Asn7=
ENST00000444314.6:n.56T>C
ENST00000524666.5:n.35T>C
ENST00000528416.5:c.21T>C	ENSP00000436901.1:p.Asn7=
ENST00000530993.5:n.46T>C
ENST00000532102.5:c.21T>C	ENSP00000434885.1:p.Asn7=
ENST00000532264.5:n.33T>C
NM_006268.4:c.21T>C	NP_006259.1:p.Asn7=
XM_005274149.1:c.21T>C	XP_005274206.1:p.Asn7=
XR_950008.1:n.68T>C
NM_001330308.1:c.21T>C	NP_001317237.1:p.Asn7=
XM_024448637.1:c.21T>C	XP_024304405.1:p.Asn7=
XR_950008.3:n.68T>C
NM_006268.5:c.21T>C MANE Select	NP_006259.1:p.Asn7=
NM_001330308.2:c.21T>C	NP_001317237.1:p.Asn7=