Canonical Allele Identifier: CA2608595013
Gene: PDSS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26697904del , CM000672.2:g.26697904del GRCh38
NC_000010.10:g.26986833del , CM000672.1:g.26986833del GRCh37
NC_000010.9:g.27026839del NCBI36
NG_008972.1:g.5239del
NG_008972.2:g.5239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376215.10:c.129+64del MANE Select ENSP00000365388.5:n.129+64del
ENST00000376215.9:c.129+64del ENSP00000365388.5:n.129+64del
NM_014317.3:c.129+64del NP_055132.2:n.129+64del
XR_428636.2:n.417+64del
XR_930486.1:n.417+64del
NM_001321978.1:c.129+64del NP_001308907.1:n.129+64del
NM_001321979.1:c.-465+64del NP_001308908.1:n.-465+64del
NM_014317.4:c.129+64del NP_055132.2:n.129+64del
XM_024447922.1:c.129+64del XP_024303690.1:n.129+64del
XR_428636.4:n.417+64del
NM_014317.5:c.129+64del MANE Select NP_055132.2:n.129+64del
NM_001321978.2:c.129+64del NP_001308907.1:n.129+64del
NM_001321979.2:c.-465+64del NP_001308908.1:n.-465+64del