Canonical Allele Identifier: CA1653786351
Gene: PDSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107210485T= , CM000668.2:g.107210485T= GRCh38
NC_000006.11:g.107531689T= , CM000668.1:g.107531689T= GRCh37
NC_000006.10:g.107638382T= NCBI36
NG_013033.1:g.254091A=

Transcript Alleles

HGVS Amino-acid change
ENST00000369037.9:c.962A= MANE Select ENSP00000358033.4:p.His321=
ENST00000369037.8:c.962A= ENSP00000358033.4:p.His321=
ENST00000449027.1:c.137A= ENSP00000392613.1:p.His46=
NM_020381.3:c.962A= NP_065114.3:p.His321=
XM_011535956.1:c.962A= XP_011534258.1:p.His321=
XM_011535957.1:c.876+1624A= XP_011534259.1:n.876+1624A=
XM_011535958.1:c.827A= XP_011534260.1:p.His276=
XM_011535959.1:c.876+1624A= XP_011534261.1:n.876+1624A=
XM_011535960.1:c.554A= XP_011534262.1:p.His185=
XM_011535961.1:c.703-16631A= XP_011534263.1:n.703-16631A=
XM_011535962.1:c.554A= XP_011534264.1:p.His185=
XM_011535956.3:c.962A= XP_011534258.1:p.His321=
XM_011535957.3:c.876+1624A= XP_011534259.1:n.876+1624A=
XM_011535958.3:c.827A= XP_011534260.1:p.His276=
XM_011535959.3:c.876+1624A= XP_011534261.1:n.876+1624A=
XM_011535960.3:c.554A= XP_011534262.1:p.His185=
XM_011535961.3:c.703-16631A= XP_011534263.1:n.703-16631A=
XM_011535962.2:c.554A= XP_011534264.1:p.His185=
XM_017011082.2:c.962A= XP_016866571.1:p.His321=
NM_020381.4:c.962A= MANE Select NP_065114.3:p.His321=