Canonical Allele Identifier: CA223956888
Community Standard Title: NM_006268.5(DPF2):c.904+45G>C
Gene: DPF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65346103G>C , CM000673.2:g.65346103G>C GRCh38
NC_000011.9:g.65113574G>C , CM000673.1:g.65113574G>C GRCh37
NC_000011.8:g.64870150G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006268.5:c.904+45G>C MANE Select NP_006259.1:n.904+45G>C
ENST00000528416.6:c.904+45G>C MANE Select ENSP00000436901.1:n.904+45G>C
NM_001330308.1:c.946+45G>C NP_001317237.1:n.946+45G>C
NM_001330308.2:c.946+45G>C NP_001317237.1:n.946+45G>C
NM_006268.4:c.904+45G>C NP_006259.1:n.904+45G>C
ENST00000252268.8:c.946+45G>C ENSP00000252268.4:n.946+45G>C
ENST00000415073.6:c.466-2747G>C ENSP00000399714.2:n.466-2747G>C
ENST00000524666.5:n.713G>C
ENST00000528416.5:c.904+45G>C ENSP00000436901.1:n.904+45G>C
ENST00000530973.1:n.686G>C
ENST00000530993.6:c.-33+45G>C ENSP00000515294.1:n.-33+45G>C
ENST00000531989.1:c.192+45G>C ENSP00000435887.1:n.192+45G>C
ENST00000532052.1:n.1673+45G>C
ENST00000703393.1:c.904+45G>C ENSP00000515285.1:n.904+45G>C
ENST00000703394.1:n.1116+45G>C
ENST00000703424.1:c.1456+45G>C ENSP00000515295.1:n.1456+45G>C
ENST00000703425.1:c.1015+45G>C ENSP00000515296.1:n.1015+45G>C
ENST00000703426.1:c.*801+45G>C ENSP00000515297.1:n.*801+45G>C
ENST00000703427.1:c.844+45G>C ENSP00000515298.1:n.844+45G>C
XM_005274149.1:c.946+45G>C XP_005274206.1:n.946+45G>C
XM_017018101.2:c.886+45G>C XP_016873590.1:n.886+45G>C
XM_017018102.1:c.844+45G>C XP_016873591.1:n.844+45G>C
XM_024448637.1:c.1456+45G>C XP_024304405.1:n.1456+45G>C
XM_024448638.1:c.1396+45G>C XP_024304406.1:n.1396+45G>C
XR_950008.1:n.872+45G>C
XR_950008.3:n.872+45G>C