Canonical Allele Identifier: CA261017574

Gene: DDHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53055547C>T , CM000676.2:g.53055547C>T	GRCh38
NC_000014.8:g.53522265C>T , CM000676.1:g.53522265C>T	GRCh37
NC_000014.7:g.52592015C>T	NCBI36
NG_042832.1:g.102782G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001160148.2:c.2245+113G>A MANE Select	NP_001153620.1:n.2245+113G>A
ENST00000673822.2:c.2245+113G>A MANE Select	ENSP00000500986.2:n.2245+113G>A
NM_001160147.1:c.2266+113G>A	NP_001153619.1:n.2266+113G>A
NM_001160147.2:c.2266+113G>A	NP_001153619.1:n.2266+113G>A
NM_001160148.1:c.2245+113G>A	NP_001153620.1:n.2245+113G>A
NM_030637.2:c.2245+113G>A	NP_085140.2:n.2245+113G>A
NM_030637.3:c.2245+113G>A	NP_085140.2:n.2245+113G>A
ENST00000323669.10:c.1654+113G>A	ENSP00000327104.6:n.1654+113G>A
ENST00000323669.9:c.2245+113G>A	ENSP00000327104.5:n.2245+113G>A
ENST00000357758.3:c.2245+113G>A	ENSP00000350401.3:n.2245+113G>A
ENST00000395606.5:c.2266+113G>A	ENSP00000378970.1:n.2266+113G>A
ENST00000555400.1:n.602+113G>A
ENST00000556027.5:n.2836+113G>A
ENST00000612692.4:c.1858+113G>A	ENSP00000483405.1:n.1858+113G>A
ENST00000673827.1:n.1921+113G>A
ENST00000673930.1:c.1633+113G>A	ENSP00000501087.1:n.1633+113G>A
ENST00000674014.1:c.1589+113G>A
ENST00000674152.1:c.1023+113G>A
XM_005268102.1:c.2347+113G>A	XP_005268159.1:n.2347+113G>A
XM_005268102.3:c.2347+113G>A	XP_005268159.1:n.2347+113G>A
XM_005268103.1:c.2266+113G>A	XP_005268160.1:n.2266+113G>A
XM_005268103.3:c.2266+113G>A	XP_005268160.1:n.2266+113G>A
XM_005268105.1:c.2116+113G>A	XP_005268162.1:n.2116+113G>A
XM_005268105.3:c.2116+113G>A	XP_005268162.1:n.2116+113G>A
XM_011537188.1:c.2368+113G>A	XP_011535490.1:n.2368+113G>A
XM_011537188.3:c.2368+113G>A	XP_011535490.1:n.2368+113G>A
XM_011537189.1:c.2368+113G>A	XP_011535491.1:n.2368+113G>A
XM_011537189.3:c.2368+113G>A	XP_011535491.1:n.2368+113G>A
XM_017021668.2:c.2347+113G>A	XP_016877157.1:n.2347+113G>A
XM_017021669.2:c.2116+113G>A	XP_016877158.1:n.2116+113G>A