Canonical Allele Identifier: CA1653773682
Gene: PDSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107245504C= , CM000668.2:g.107245504C= GRCh38
NC_000006.11:g.107566708C= , CM000668.1:g.107566708C= GRCh37
NC_000006.10:g.107673401C= NCBI36
NG_013033.1:g.219072G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369037.9:c.702+44G= MANE Select ENSP00000358033.4:n.702+44G=
ENST00000369037.8:c.702+44G= ENSP00000358033.4:n.702+44G=
NM_020381.3:c.702+44G= NP_065114.3:n.702+44G=
XM_011535956.1:c.702+44G= XP_011534258.1:n.702+44G=
XM_011535957.1:c.702+44G= XP_011534259.1:n.702+44G=
XM_011535958.1:c.567+44G= XP_011534260.1:n.567+44G=
XM_011535959.1:c.702+44G= XP_011534261.1:n.702+44G=
XM_011535960.1:c.294+44G= XP_011534262.1:n.294+44G=
XM_011535961.1:c.702+44G= XP_011534263.1:n.702+44G=
XM_011535962.1:c.294+44G= XP_011534264.1:n.294+44G=
XM_011535956.3:c.702+44G= XP_011534258.1:n.702+44G=
XM_011535957.3:c.702+44G= XP_011534259.1:n.702+44G=
XM_011535958.3:c.567+44G= XP_011534260.1:n.567+44G=
XM_011535959.3:c.702+44G= XP_011534261.1:n.702+44G=
XM_011535960.3:c.294+44G= XP_011534262.1:n.294+44G=
XM_011535961.3:c.702+44G= XP_011534263.1:n.702+44G=
XM_011535962.2:c.294+44G= XP_011534264.1:n.294+44G=
XM_017011082.2:c.702+44G= XP_016866571.1:n.702+44G=
NM_020381.4:c.702+44G= MANE Select NP_065114.3:n.702+44G=