Canonical Allele Identifier: CA2838276396

Gene: DPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43972375del , CM000663.2:g.43972375del	GRCh38
NC_000001.10:g.44438047del , CM000663.1:g.44438047del	GRCh37
NC_000001.9:g.44210634del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255108.8:c.1346-40del MANE Select	ENSP00000255108.3:n.1346-40del
ENST00000255108.7:c.1346-40del	ENSP00000255108.3:n.1346-40del
ENST00000396758.6:c.662-40del	ENSP00000379981.2:n.662-40del
ENST00000459879.1:c.665-40del	ENSP00000432162.1:n.665-40del
ENST00000495421.1:c.*1012-40del	ENSP00000431944.1:n.*1012-40del
ENST00000524776.5:c.*678-40del	ENSP00000434977.1:n.*678-40del
ENST00000527319.1:c.250-40del
NM_001039589.1:c.662-40del	NP_001034678.1:n.662-40del
NM_001384.4:c.1346-40del	NP_001375.2:n.1346-40del
XM_005270559.2:c.1118-40del	XP_005270616.1:n.1118-40del
XM_011540866.1:c.767-40del	XP_011539168.1:n.767-40del
XM_011540867.1:c.767-40del	XP_011539169.1:n.767-40del
NM_001319165.1:c.1118-40del	NP_001306094.1:n.1118-40del
NM_001319166.1:c.1073-40del	NP_001306095.1:n.1073-40del
NM_001319167.1:c.767-40del	NP_001306096.1:n.767-40del
NM_001319168.1:c.1118-40del	NP_001306097.1:n.1118-40del
NM_001319169.1:c.941-40del	NP_001306098.1:n.941-40del
NM_001319170.1:c.767-40del	NP_001306099.1:n.767-40del
NM_001319171.1:c.902-40del	NP_001306100.1:n.902-40del
XM_017000502.2:c.1386del	XP_016855991.1:p.Arg463AspfsTer7
NM_001384.5:c.1346-40del MANE Select	NP_001375.2:n.1346-40del
NM_001039589.2:c.662-40del	NP_001034678.1:n.662-40del
NM_001319165.2:c.1118-40del	NP_001306094.1:n.1118-40del
NM_001319166.2:c.1073-40del	NP_001306095.1:n.1073-40del
NM_001319167.2:c.767-40del	NP_001306096.1:n.767-40del
NM_001319168.2:c.1118-40del	NP_001306097.1:n.1118-40del
NM_001319169.2:c.941-40del	NP_001306098.1:n.941-40del
NM_001319170.2:c.767-40del	NP_001306099.1:n.767-40del
NM_001319171.2:c.902-40del	NP_001306100.1:n.902-40del