Canonical Allele Identifier: CA2573147658
Community Standard Title: NM_006268.5(DPF2):c.194-3C>A
Gene: DPF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65340963C>A , CM000673.2:g.65340963C>A GRCh38
NC_000011.9:g.65108434C>A , CM000673.1:g.65108434C>A GRCh37
NC_000011.8:g.64865010C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006268.5:c.194-3C>A MANE Select NP_006259.1:n.194-3C>A
ENST00000528416.6:c.194-3C>A MANE Select ENSP00000436901.1:n.194-3C>A
NM_001330308.1:c.194-3C>A NP_001317237.1:n.194-3C>A
NM_001330308.2:c.194-3C>A NP_001317237.1:n.194-3C>A
NM_006268.4:c.194-3C>A NP_006259.1:n.194-3C>A
ENST00000252268.8:c.194-3C>A ENSP00000252268.4:n.194-3C>A
ENST00000415073.6:c.194-3C>A ENSP00000399714.2:n.194-3C>A
ENST00000444314.6:n.229-3C>A
ENST00000524666.5:n.47-3C>A
ENST00000528416.5:c.194-3C>A ENSP00000436901.1:n.194-3C>A
ENST00000530993.5:n.58-3C>A
ENST00000530993.6:c.-785-3C>A ENSP00000515294.1:n.-785-3C>A
ENST00000532102.5:c.194-3C>A ENSP00000434885.1:n.194-3C>A
ENST00000532264.5:n.45-3C>A
ENST00000703393.1:c.194-3C>A ENSP00000515285.1:n.194-3C>A
ENST00000703394.1:n.238-3C>A
ENST00000703424.1:c.194-3C>A ENSP00000515295.1:n.194-3C>A
ENST00000703425.1:c.263-3C>A ENSP00000515296.1:n.263-3C>A
ENST00000703426.1:c.*49-3C>A ENSP00000515297.1:n.*49-3C>A
ENST00000703427.1:c.134-3C>A ENSP00000515298.1:n.134-3C>A
XM_005274149.1:c.194-3C>A XP_005274206.1:n.194-3C>A
XM_017018101.2:c.134-3C>A XP_016873590.1:n.134-3C>A
XM_017018102.1:c.134-3C>A XP_016873591.1:n.134-3C>A
XM_024448637.1:c.194-3C>A XP_024304405.1:n.194-3C>A
XM_024448638.1:c.134-3C>A XP_024304406.1:n.134-3C>A
XR_950008.1:n.241-3C>A
XR_950008.3:n.241-3C>A