Canonical Allele Identifier: CA6095292

Gene: DPF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65343795T>C , CM000673.2:g.65343795T>C	GRCh38
NC_000011.9:g.65111266T>C , CM000673.1:g.65111266T>C	GRCh37
NC_000011.8:g.64867842T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530993.6:c.-463T>C	ENSP00000515294.1:n.-463T>C
ENST00000703393.1:c.516T>C	ENSP00000515285.1:p.Tyr172=
ENST00000703394.1:n.560T>C
ENST00000703424.1:c.516T>C	ENSP00000515295.1:p.Tyr172=
ENST00000703425.1:c.585T>C	ENSP00000515296.1:p.Tyr195=
ENST00000703426.1:c.*371T>C	ENSP00000515297.1:n.*371T>C
ENST00000703427.1:c.456T>C	ENSP00000515298.1:p.Tyr152=
ENST00000528416.6:c.516T>C MANE Select	ENSP00000436901.1:p.Tyr172=
ENST00000252268.8:c.516T>C	ENSP00000252268.4:p.Tyr172=
ENST00000415073.6:c.465+2233T>C	ENSP00000399714.2:n.465+2233T>C
ENST00000524666.5:n.359T>C
ENST00000528416.5:c.516T>C	ENSP00000436901.1:p.Tyr172=
ENST00000530973.1:n.127T>C
ENST00000530993.5:n.380T>C
ENST00000532102.5:c.*31T>C	ENSP00000434885.1:n.*31T>C
ENST00000532264.5:n.367T>C
ENST00000532492.1:n.291T>C
NM_006268.4:c.516T>C	NP_006259.1:p.Tyr172=
XM_005274149.1:c.516T>C	XP_005274206.1:p.Tyr172=
XR_950008.1:n.563T>C
NM_001330308.1:c.516T>C	NP_001317237.1:p.Tyr172=
XM_017018101.2:c.456T>C	XP_016873590.1:p.Tyr152=
XM_017018102.1:c.456T>C	XP_016873591.1:p.Tyr152=
XM_024448637.1:c.516T>C	XP_024304405.1:p.Tyr172=
XM_024448638.1:c.456T>C	XP_024304406.1:p.Tyr152=
XR_950008.3:n.563T>C
NM_006268.5:c.516T>C MANE Select	NP_006259.1:p.Tyr172=
NM_001330308.2:c.516T>C	NP_001317237.1:p.Tyr172=