Canonical Allele Identifier: CA381882576
Gene: GDPD5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.75456792C>T , CM000673.2:g.75456792C>T GRCh38
NC_000011.9:g.75167837C>T , CM000673.1:g.75167837C>T GRCh37
NC_000011.8:g.74845485C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336898.8:c.340G>A MANE Select ENSP00000337972.3:p.Val114Met
ENST00000336898.7:c.340G>A ENSP00000337972.3:p.Val114Met
ENST00000443276.6:c.340G>A ENSP00000396535.2:p.Val114Met
ENST00000527322.5:n.119G>A
ENST00000527820.5:c.340G>A ENSP00000437123.1:p.Val114Met
ENST00000528031.1:n.474G>A
ENST00000529721.5:c.340G>A ENSP00000433214.1:p.Val114Met
ENST00000533784.5:c.118-7182G>A ENSP00000437049.1:n.118-7182G>A
NM_030792.6:c.340G>A NP_110419.5:p.Val114Met
XM_006718697.2:c.340G>A XP_006718760.1:p.Val114Met
XM_011545275.1:c.340G>A XP_011543577.1:p.Val114Met
XM_011545276.1:c.340G>A XP_011543578.1:p.Val114Met
XM_011545277.1:c.340G>A XP_011543579.1:p.Val114Met
XM_011545278.1:c.340G>A XP_011543580.1:p.Val114Met
XM_011545279.1:c.340G>A XP_011543581.1:p.Val114Met
XM_011545280.1:c.14G>A XP_011543582.1:p.Arg5His
NM_001351168.1:c.-554G>A NP_001338097.1:n.-554G>A
NM_030792.7:c.340G>A NP_110419.5:p.Val114Met
XM_006718697.3:c.340G>A XP_006718760.1:p.Val114Met
XM_011545276.2:c.340G>A XP_011543578.1:p.Val114Met
XM_011545277.2:c.340G>A XP_011543579.1:p.Val114Met
XM_011545278.2:c.340G>A XP_011543580.1:p.Val114Met
XM_011545279.2:c.340G>A XP_011543581.1:p.Val114Met
NM_030792.8:c.340G>A MANE Select NP_110419.5:p.Val114Met