Canonical Allele Identifier: CA2573149989

Gene: DDHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.53046957G>C , CM000676.2:g.53046957G>C	GRCh38
NC_000014.8:g.53513675G>C , CM000676.1:g.53513675G>C	GRCh37
NC_000014.7:g.52583425G>C	NCBI36
NG_042832.1:g.111372C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001160148.2:c.2522-8C>G MANE Select	NP_001153620.1:n.2522-8C>G
ENST00000673822.2:c.2522-8C>G MANE Select	ENSP00000500986.2:n.2522-8C>G
NM_001160147.1:c.2459-8C>G	NP_001153619.1:n.2459-8C>G
NM_001160147.2:c.2459-8C>G	NP_001153619.1:n.2459-8C>G
NM_001160148.1:c.2522-8C>G	NP_001153620.1:n.2522-8C>G
NM_030637.2:c.2438-8C>G	NP_085140.2:n.2438-8C>G
NM_030637.3:c.2438-8C>G	NP_085140.2:n.2438-8C>G
ENST00000323669.10:c.1847-8C>G	ENSP00000327104.6:n.1847-8C>G
ENST00000323669.9:c.2522-8C>G	ENSP00000327104.5:n.2522-8C>G
ENST00000357758.3:c.2438-8C>G	ENSP00000350401.3:n.2438-8C>G
ENST00000395606.5:c.2459-8C>G	ENSP00000378970.1:n.2459-8C>G
ENST00000556027.5:n.3029-8C>G
ENST00000612692.4:c.2135-8C>G	ENSP00000483405.1:n.2135-8C>G
ENST00000673827.1:n.2114-8C>G
ENST00000673930.1:c.1826-8C>G	ENSP00000501087.1:n.1826-8C>G
ENST00000674014.1:c.1782-8C>G
ENST00000674152.1:c.1216-8C>G
XM_005268102.1:c.2624-8C>G	XP_005268159.1:n.2624-8C>G
XM_005268102.3:c.2624-8C>G	XP_005268159.1:n.2624-8C>G
XM_005268103.1:c.2543-8C>G	XP_005268160.1:n.2543-8C>G
XM_005268103.3:c.2543-8C>G	XP_005268160.1:n.2543-8C>G
XM_005268105.1:c.2393-8C>G	XP_005268162.1:n.2393-8C>G
XM_005268105.3:c.2393-8C>G	XP_005268162.1:n.2393-8C>G
XM_011537188.1:c.2645-8C>G	XP_011535490.1:n.2645-8C>G
XM_011537188.3:c.2645-8C>G	XP_011535490.1:n.2645-8C>G
XM_011537189.1:c.2561-8C>G	XP_011535491.1:n.2561-8C>G
XM_011537189.3:c.2561-8C>G	XP_011535491.1:n.2561-8C>G
XM_017021668.2:c.2540-8C>G	XP_016877157.1:n.2540-8C>G
XM_017021669.2:c.2309-8C>G	XP_016877158.1:n.2309-8C>G