Canonical Allele Identifier: CA6190653

Gene: GDPD5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75477620G>A , CM000673.2:g.75477620G>A	GRCh38
NC_000011.9:g.75188665G>A , CM000673.1:g.75188665G>A	GRCh37
NC_000011.8:g.74866313G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030792.8:c.116C>T MANE Select	NP_110419.5:p.Pro39Leu
ENST00000336898.8:c.116C>T MANE Select	ENSP00000337972.3:p.Pro39Leu
NM_001351168.1:c.-778C>T	NP_001338097.1:n.-778C>T
NM_030792.6:c.116C>T	NP_110419.5:p.Pro39Leu
NM_030792.7:c.116C>T	NP_110419.5:p.Pro39Leu
ENST00000336898.7:c.116C>T	ENSP00000337972.3:p.Pro39Leu
ENST00000443276.6:c.116C>T	ENSP00000396535.2:p.Pro39Leu
ENST00000527820.5:c.116C>T	ENSP00000437123.1:p.Pro39Leu
ENST00000528031.1:n.250C>T
ENST00000529721.5:c.116C>T	ENSP00000433214.1:p.Pro39Leu
ENST00000532435.5:c.116C>T	ENSP00000433727.1:p.Pro39Leu
ENST00000533784.5:c.116C>T	ENSP00000437049.1:p.Pro39Leu
XM_006718697.2:c.116C>T	XP_006718760.1:p.Pro39Leu
XM_006718697.3:c.116C>T	XP_006718760.1:p.Pro39Leu
XM_011545275.1:c.116C>T	XP_011543577.1:p.Pro39Leu
XM_011545276.1:c.116C>T	XP_011543578.1:p.Pro39Leu
XM_011545276.2:c.116C>T	XP_011543578.1:p.Pro39Leu
XM_011545277.1:c.116C>T	XP_011543579.1:p.Pro39Leu
XM_011545277.2:c.116C>T	XP_011543579.1:p.Pro39Leu
XM_011545278.1:c.116C>T	XP_011543580.1:p.Pro39Leu
XM_011545278.2:c.116C>T	XP_011543580.1:p.Pro39Leu
XM_011545279.1:c.116C>T	XP_011543581.1:p.Pro39Leu
XM_011545279.2:c.116C>T	XP_011543581.1:p.Pro39Leu
XM_011545280.1:c.-211C>T	XP_011543582.1:n.-211C>T