Canonical Allele Identifier: CA7191039

Gene: DDHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53055745G>A , CM000676.2:g.53055745G>A	GRCh38
NC_000014.8:g.53522463G>A , CM000676.1:g.53522463G>A	GRCh37
NC_000014.7:g.52592213G>A	NCBI36
NG_042832.1:g.102584C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001160148.2:c.2160C>T MANE Select	NP_001153620.1:p.Thr720=
ENST00000673822.2:c.2160C>T MANE Select	ENSP00000500986.2:p.Thr720=
NM_001160147.1:c.2181C>T	NP_001153619.1:p.Thr727=
NM_001160147.2:c.2181C>T	NP_001153619.1:p.Thr727=
NM_001160148.1:c.2160C>T	NP_001153620.1:p.Thr720=
NM_030637.2:c.2160C>T	NP_085140.2:p.Thr720=
NM_030637.3:c.2160C>T	NP_085140.2:p.Thr720=
ENST00000323669.10:c.1569C>T	ENSP00000327104.6:p.Thr523=
ENST00000323669.9:c.2160C>T	ENSP00000327104.5:p.Thr720=
ENST00000357758.3:c.2160C>T	ENSP00000350401.3:p.Thr720=
ENST00000395606.5:c.2181C>T	ENSP00000378970.1:p.Thr727=
ENST00000555400.1:n.517C>T
ENST00000556027.5:n.2751C>T
ENST00000612692.4:c.1773C>T	ENSP00000483405.1:p.Thr591=
ENST00000673827.1:n.1836C>T
ENST00000673930.1:c.1548C>T	ENSP00000501087.1:p.Thr516=
ENST00000674014.1:c.1504C>T
ENST00000674152.1:c.938C>T
XM_005268102.1:c.2262C>T	XP_005268159.1:p.Thr754=
XM_005268102.3:c.2262C>T	XP_005268159.1:p.Thr754=
XM_005268103.1:c.2181C>T	XP_005268160.1:p.Thr727=
XM_005268103.3:c.2181C>T	XP_005268160.1:p.Thr727=
XM_005268105.1:c.2031C>T	XP_005268162.1:p.Thr677=
XM_005268105.3:c.2031C>T	XP_005268162.1:p.Thr677=
XM_011537188.1:c.2283C>T	XP_011535490.1:p.Thr761=
XM_011537188.3:c.2283C>T	XP_011535490.1:p.Thr761=
XM_011537189.1:c.2283C>T	XP_011535491.1:p.Thr761=
XM_011537189.3:c.2283C>T	XP_011535491.1:p.Thr761=
XM_017021668.2:c.2262C>T	XP_016877157.1:p.Thr754=
XM_017021669.2:c.2031C>T	XP_016877158.1:p.Thr677=