Canonical Allele Identifier: CA2608594944
Gene: PDSS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26697866del , CM000672.2:g.26697866del GRCh38
NC_000010.10:g.26986795del , CM000672.1:g.26986795del GRCh37
NC_000010.9:g.27026801del NCBI36
NG_008972.1:g.5201del
NG_008972.2:g.5201del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376215.10:c.129+26del MANE Select ENSP00000365388.5:n.129+26del
ENST00000376215.9:c.129+26del ENSP00000365388.5:n.129+26del
NM_014317.3:c.129+26del NP_055132.2:n.129+26del
XR_428636.2:n.417+26del
XR_930486.1:n.417+26del
NM_001321978.1:c.129+26del NP_001308907.1:n.129+26del
NM_001321979.1:c.-465+26del NP_001308908.1:n.-465+26del
NM_014317.4:c.129+26del NP_055132.2:n.129+26del
XM_024447922.1:c.129+26del XP_024303690.1:n.129+26del
XR_428636.4:n.417+26del
NM_014317.5:c.129+26del MANE Select NP_055132.2:n.129+26del
NM_001321978.2:c.129+26del NP_001308907.1:n.129+26del
NM_001321979.2:c.-465+26del NP_001308908.1:n.-465+26del