Canonical Allele Identifier: CA1898170361
Gene: PDSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26697820G= , CM000672.2:g.26697820G= GRCh38
NC_000010.10:g.26986749G= , CM000672.1:g.26986749G= GRCh37
NC_000010.9:g.27026755G= NCBI36
NG_008972.1:g.5155G=
NG_008972.2:g.5155G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376215.10:c.109G= MANE Select ENSP00000365388.5:p.Ala37=
ENST00000376215.9:c.109G= ENSP00000365388.5:p.Ala37=
NM_014317.3:c.109G= NP_055132.2:p.Ala37=
XR_428636.2:n.397G=
XR_930486.1:n.397G=
NM_001321978.1:c.109G= NP_001308907.1:p.Ala37=
NM_001321979.1:c.-485G= NP_001308908.1:n.-485G=
NM_014317.4:c.109G= NP_055132.2:p.Ala37=
XM_024447922.1:c.109G= XP_024303690.1:p.Ala37=
XR_428636.4:n.397G=
NM_014317.5:c.109G= MANE Select NP_055132.2:p.Ala37=
NM_001321978.2:c.109G= NP_001308907.1:p.Ala37=
NM_001321979.2:c.-485G= NP_001308908.1:n.-485G=