Canonical Allele Identifier: CA4716015

Gene: DDHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38238153G>T , CM000670.2:g.38238153G>T	GRCh38
NC_000008.10:g.38095671G>T , CM000670.1:g.38095671G>T	GRCh37
NC_000008.9:g.38214828G>T	NCBI36
NG_033875.1:g.11663G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397166.7:c.566G>T MANE Select	ENSP00000380352.2:p.Gly189Val
ENST00000397166.6:c.566G>T	ENSP00000380352.2:p.Gly189Val
ENST00000519857.5:n.763G>T
ENST00000520272.6:c.566G>T	ENSP00000429932.2:p.Gly189Val
ENST00000526237.5:c.*123G>T	ENSP00000436994.1:n.*123G>T
ENST00000527415.5:c.411+526G>T	ENSP00000432024.1:n.411+526G>T
ENST00000532222.5:c.566G>T	ENSP00000433578.1:p.Gly189Val
NM_001164232.1:c.566G>T	NP_001157704.1:p.Gly189Val
NM_001164234.1:c.566G>T	NP_001157706.1:p.Gly189Val
NM_015214.2:c.566G>T	NP_056029.2:p.Gly189Val
XM_005273454.1:c.566G>T	XP_005273511.1:p.Gly189Val
XM_005273455.2:c.566G>T	XP_005273512.1:p.Gly189Val
XM_005273456.2:c.566G>T	XP_005273513.1:p.Gly189Val
XM_011544455.1:c.566G>T	XP_011542757.1:p.Gly189Val
XM_011544456.1:c.566G>T	XP_011542758.1:p.Gly189Val
XR_247123.1:n.1091G>T
XR_949383.1:n.1091G>T
XR_949384.1:n.1091G>T
XR_949385.1:n.1091G>T
XR_949386.1:n.1091G>T
XR_949387.1:n.1091G>T
NM_001362911.1:c.566G>T	NP_001349840.1:p.Gly189Val
NM_001362912.1:c.566G>T	NP_001349841.1:p.Gly189Val
NM_001362913.1:c.566G>T	NP_001349842.1:p.Gly189Val
NM_001362914.1:c.566G>T	NP_001349843.1:p.Gly189Val
NR_156416.1:n.943G>T
NR_156417.1:n.943G>T
XM_011544456.2:c.566G>T	XP_011542758.1:p.Gly189Val
XM_017013255.2:c.-420G>T	XP_016868744.1:n.-420G>T
XR_001745504.2:n.849G>T
XR_001745506.2:n.849G>T
NM_001362911.2:c.566G>T	NP_001349840.1:p.Gly189Val
NM_001362912.2:c.566G>T	NP_001349841.1:p.Gly189Val
NM_015214.3:c.566G>T MANE Select	NP_056029.2:p.Gly189Val
NR_156417.2:n.849G>T
NM_001164232.2:c.566G>T	NP_001157704.1:p.Gly189Val
NM_001164234.2:c.566G>T	NP_001157706.1:p.Gly189Val
NM_001362913.2:c.566G>T	NP_001349842.1:p.Gly189Val
NM_001362914.2:c.566G>T	NP_001349843.1:p.Gly189Val
NR_156416.2:n.849G>T