Canonical Allele Identifier: CA1898170008
Gene: PDSS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.26697705T= , CM000672.2:g.26697705T= GRCh38
NC_000010.10:g.26986634T= , CM000672.1:g.26986634T= GRCh37
NC_000010.9:g.27026640T= NCBI36
NG_008972.1:g.5040T=
NG_008972.2:g.5040T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376215.10:c.-7T= MANE Select ENSP00000365388.5:n.-7T=
ENST00000376215.9:c.-7T= ENSP00000365388.5:n.-7T=
NM_014317.3:c.-7T= NP_055132.2:n.-7T=
XR_428636.2:n.282T=
XR_930486.1:n.282T=
NM_001321978.1:c.-7T= NP_001308907.1:n.-7T=
NM_001321979.1:c.-600T= NP_001308908.1:n.-600T=
NM_014317.4:c.-7T= NP_055132.2:n.-7T=
XM_024447922.1:c.-7T= XP_024303690.1:n.-7T=
XR_428636.4:n.282T=
NM_014317.5:c.-7T= MANE Select NP_055132.2:n.-7T=
NM_001321978.2:c.-7T= NP_001308907.1:n.-7T=
NM_001321979.2:c.-600T= NP_001308908.1:n.-600T=