Canonical Allele Identifier: CA1653786354
Gene: PDSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107210496A= , CM000668.2:g.107210496A= GRCh38
NC_000006.11:g.107531700A= , CM000668.1:g.107531700A= GRCh37
NC_000006.10:g.107638393A= NCBI36
NG_013033.1:g.254080T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369037.9:c.951T= MANE Select ENSP00000358033.4:p.Pro317=
ENST00000369037.8:c.951T= ENSP00000358033.4:p.Pro317=
ENST00000449027.1:c.126T= ENSP00000392613.1:p.Pro42=
NM_020381.3:c.951T= NP_065114.3:p.Pro317=
XM_011535956.1:c.951T= XP_011534258.1:p.Pro317=
XM_011535957.1:c.876+1613T= XP_011534259.1:n.876+1613T=
XM_011535958.1:c.816T= XP_011534260.1:p.Pro272=
XM_011535959.1:c.876+1613T= XP_011534261.1:n.876+1613T=
XM_011535960.1:c.543T= XP_011534262.1:p.Pro181=
XM_011535961.1:c.703-16642T= XP_011534263.1:n.703-16642T=
XM_011535962.1:c.543T= XP_011534264.1:p.Pro181=
XM_011535956.3:c.951T= XP_011534258.1:p.Pro317=
XM_011535957.3:c.876+1613T= XP_011534259.1:n.876+1613T=
XM_011535958.3:c.816T= XP_011534260.1:p.Pro272=
XM_011535959.3:c.876+1613T= XP_011534261.1:n.876+1613T=
XM_011535960.3:c.543T= XP_011534262.1:p.Pro181=
XM_011535961.3:c.703-16642T= XP_011534263.1:n.703-16642T=
XM_011535962.2:c.543T= XP_011534264.1:p.Pro181=
XM_017011082.2:c.951T= XP_016866571.1:p.Pro317=
NM_020381.4:c.951T= MANE Select NP_065114.3:p.Pro317=