Canonical Allele Identifier: CA7191584
Gene: DDHD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53152963C>T , CM000676.2:g.53152963C>T GRCh38
NC_000014.8:g.53619681C>T , CM000676.1:g.53619681C>T GRCh37
NC_000014.7:g.52689431C>T NCBI36
NG_042832.1:g.5366G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001160148.2:c.136G>A MANE Select NP_001153620.1:p.Gly46Ser
ENST00000673822.2:c.136G>A MANE Select ENSP00000500986.2:p.Gly46Ser
NM_001160147.1:c.136G>A NP_001153619.1:p.Gly46Ser
NM_001160147.2:c.136G>A NP_001153619.1:p.Gly46Ser
NM_001160148.1:c.136G>A NP_001153620.1:p.Gly46Ser
NM_030637.2:c.136G>A NP_085140.2:p.Gly46Ser
NM_030637.3:c.136G>A NP_085140.2:p.Gly46Ser
ENST00000323669.9:c.136G>A ENSP00000327104.5:p.Gly46Ser
ENST00000357758.3:c.136G>A ENSP00000350401.3:p.Gly46Ser
ENST00000395606.5:c.136G>A ENSP00000378970.1:p.Gly46Ser
ENST00000612692.4:c.136G>A ENSP00000483405.1:p.Gly46Ser
XM_005268102.1:c.136G>A XP_005268159.1:p.Gly46Ser
XM_005268102.3:c.136G>A XP_005268159.1:p.Gly46Ser
XM_005268103.1:c.136G>A XP_005268160.1:p.Gly46Ser
XM_005268103.3:c.136G>A XP_005268160.1:p.Gly46Ser
XM_005268105.1:c.136G>A XP_005268162.1:p.Gly46Ser
XM_005268105.3:c.136G>A XP_005268162.1:p.Gly46Ser
XM_011537188.1:c.136G>A XP_011535490.1:p.Gly46Ser
XM_011537188.3:c.136G>A XP_011535490.1:p.Gly46Ser
XM_011537189.1:c.136G>A XP_011535491.1:p.Gly46Ser
XM_011537189.3:c.136G>A XP_011535491.1:p.Gly46Ser
XM_017021668.2:c.136G>A XP_016877157.1:p.Gly46Ser
XM_017021669.2:c.136G>A XP_016877158.1:p.Gly46Ser