Canonical Allele Identifier: CA581123338

Gene: DDHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38234784_38234785dup , CM000670.2:g.38234784_38234785dup	GRCh38
NC_000008.10:g.38092302_38092303dup , CM000670.1:g.38092302_38092303dup	GRCh37
NC_000008.9:g.38211459_38211460dup	NCBI36
NG_033875.1:g.8294_8295dup

Transcript Alleles

HGVS	Amino-acid Change
NM_015214.3:c.411+200_411+201dup MANE Select	NP_056029.2:n.411+200_411+201dup
ENST00000397166.7:c.411+200_411+201dup MANE Select	ENSP00000380352.2:n.411+200_411+201dup
NM_001164232.1:c.411+200_411+201dup	NP_001157704.1:n.411+200_411+201dup
NM_001164232.2:c.411+200_411+201dup	NP_001157704.1:n.411+200_411+201dup
NM_001164234.1:c.411+200_411+201dup	NP_001157706.1:n.411+200_411+201dup
NM_001164234.2:c.411+200_411+201dup	NP_001157706.1:n.411+200_411+201dup
NM_001362911.1:c.411+200_411+201dup	NP_001349840.1:n.411+200_411+201dup
NM_001362911.2:c.411+200_411+201dup	NP_001349840.1:n.411+200_411+201dup
NM_001362912.1:c.411+200_411+201dup	NP_001349841.1:n.411+200_411+201dup
NM_001362912.2:c.411+200_411+201dup	NP_001349841.1:n.411+200_411+201dup
NM_001362913.1:c.411+200_411+201dup	NP_001349842.1:n.411+200_411+201dup
NM_001362913.2:c.411+200_411+201dup	NP_001349842.1:n.411+200_411+201dup
NM_001362914.1:c.411+200_411+201dup	NP_001349843.1:n.411+200_411+201dup
NM_001362914.2:c.411+200_411+201dup	NP_001349843.1:n.411+200_411+201dup
NM_015214.2:c.411+200_411+201dup	NP_056029.2:n.411+200_411+201dup
NR_156416.1:n.788+200_788+201dup
NR_156416.2:n.694+200_694+201dup
NR_156417.1:n.788+200_788+201dup
NR_156417.2:n.694+200_694+201dup
ENST00000397166.6:c.411+200_411+201dup	ENSP00000380352.2:n.411+200_411+201dup
ENST00000519857.5:n.608+200_608+201dup
ENST00000520272.6:c.411+200_411+201dup	ENSP00000429932.2:n.411+200_411+201dup
ENST00000526237.5:c.220+1570_220+1571dup	ENSP00000436994.1:n.220+1570_220+1571dup
ENST00000526370.1:n.490+274_490+275dup
ENST00000527415.5:c.321+200_321+201dup	ENSP00000432024.1:n.321+200_321+201dup
ENST00000527834.5:c.411+200_411+201dup	ENSP00000432433.1:n.411+200_411+201dup
ENST00000528358.5:c.405+200_405+201dup	ENSP00000433118.1:n.405+200_405+201dup
ENST00000529642.1:c.123+200_123+201dup	ENSP00000436444.1:n.123+200_123+201dup
ENST00000532222.5:c.411+200_411+201dup	ENSP00000433578.1:n.411+200_411+201dup
XM_005273454.1:c.411+200_411+201dup	XP_005273511.1:n.411+200_411+201dup
XM_005273455.2:c.411+200_411+201dup	XP_005273512.1:n.411+200_411+201dup
XM_005273456.2:c.411+200_411+201dup	XP_005273513.1:n.411+200_411+201dup
XM_011544455.1:c.411+200_411+201dup	XP_011542757.1:n.411+200_411+201dup
XM_011544456.1:c.411+200_411+201dup	XP_011542758.1:n.411+200_411+201dup
XM_011544456.2:c.411+200_411+201dup	XP_011542758.1:n.411+200_411+201dup
XM_017013255.2:c.-575+200_-575+201dup	XP_016868744.1:n.-575+200_-575+201dup
XR_001745504.2:n.694+200_694+201dup
XR_001745506.2:n.694+200_694+201dup
XR_247123.1:n.936+200_936+201dup
XR_949383.1:n.936+200_936+201dup
XR_949384.1:n.936+200_936+201dup
XR_949385.1:n.936+200_936+201dup
XR_949386.1:n.936+200_936+201dup
XR_949387.1:n.936+200_936+201dup