Canonical Allele Identifier: CA1979165237
Community Standard Title: NM_006268.5(DPF2):c.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
Gene: DPF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65346073_65346098delinsGAAGGCTGCTGCTTTGCCCAGTCCCC , CM000673.2:g.65346073_65346098delinsGAAGGCTGCTGCTTTGCCCAGTCCCC GRCh38
NC_000011.9:g.65113544_65113569delinsGAAGGCTGCTGCTTTGCCCAGTCCCC , CM000673.1:g.65113544_65113569delinsGAAGGCTGCTGCTTTGCCCAGTCCCC GRCh37
NC_000011.8:g.64870120_64870145delinsGAAGGCTGCTGCTTTGCCCAGTCCCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_006268.5:c.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC MANE Select NP_006259.1:n.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
ENST00000528416.6:c.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC MANE Select ENSP00000436901.1:n.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGT...
NM_001330308.1:c.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC NP_001317237.1:n.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGTCCC...
NM_001330308.2:c.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC NP_001317237.1:n.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGTCCC...
NM_006268.4:c.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC NP_006259.1:n.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
ENST00000252268.8:c.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000252268.4:n.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGT...
ENST00000415073.6:c.466-2777_466-2752delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000399714.2:n.466-2777_466-2752delinsGAAGGCTGCTGCTTTGCC...
ENST00000524666.5:n.683_708delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
ENST00000528416.5:c.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000436901.1:n.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGT...
ENST00000530973.1:n.656_681delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
ENST00000530993.6:c.-33+15_-33+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000515294.1:n.-33+15_-33+40delinsGAAGGCTGCTGCTTTGCCCAGT...
ENST00000531989.1:c.192+15_192+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000435887.1:n.192+15_192+40delinsGAAGGCTGCTGCTTTGCCCAGT...
ENST00000532052.1:n.1673+15_1673+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
ENST00000703393.1:c.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000515285.1:n.904+15_904+40delinsGAAGGCTGCTGCTTTGCCCAGT...
ENST00000703394.1:n.1116+15_1116+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
ENST00000703424.1:c.1456+15_1456+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000515295.1:n.1456+15_1456+40delinsGAAGGCTGCTGCTTTGCCCA...
ENST00000703425.1:c.1015+15_1015+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000515296.1:n.1015+15_1015+40delinsGAAGGCTGCTGCTTTGCCCA...
ENST00000703426.1:c.*801+15_*801+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000515297.1:n.*801+15_*801+40delinsGAAGGCTGCTGCTTTGCCCA...
ENST00000703427.1:c.844+15_844+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC ENSP00000515298.1:n.844+15_844+40delinsGAAGGCTGCTGCTTTGCCCAGT...
XM_005274149.1:c.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC XP_005274206.1:n.946+15_946+40delinsGAAGGCTGCTGCTTTGCCCAGTCCC...
XM_017018101.2:c.886+15_886+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC XP_016873590.1:n.886+15_886+40delinsGAAGGCTGCTGCTTTGCCCAGTCCC...
XM_017018102.1:c.844+15_844+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC XP_016873591.1:n.844+15_844+40delinsGAAGGCTGCTGCTTTGCCCAGTCCC...
XM_024448637.1:c.1456+15_1456+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC XP_024304405.1:n.1456+15_1456+40delinsGAAGGCTGCTGCTTTGCCCAGTC...
XM_024448638.1:c.1396+15_1396+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC XP_024304406.1:n.1396+15_1396+40delinsGAAGGCTGCTGCTTTGCCCAGTC...
XR_950008.1:n.872+15_872+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC
XR_950008.3:n.872+15_872+40delinsGAAGGCTGCTGCTTTGCCCAGTCCCC