Canonical Allele Identifier: CA1653786376

Gene: PDSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107210551G= , CM000668.2:g.107210551G=	GRCh38
NC_000006.11:g.107531755G= , CM000668.1:g.107531755G=	GRCh37
NC_000006.10:g.107638448G=	NCBI36
NG_013033.1:g.254025C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369037.9:c.896C= MANE Select	ENSP00000358033.4:p.Pro299=
ENST00000369037.8:c.896C=	ENSP00000358033.4:p.Pro299=
ENST00000449027.1:c.71C=	ENSP00000392613.1:p.Pro24=
NM_020381.3:c.896C=	NP_065114.3:p.Pro299=
XM_011535956.1:c.896C=	XP_011534258.1:p.Pro299=
XM_011535957.1:c.876+1558C=	XP_011534259.1:n.876+1558C=
XM_011535958.1:c.761C=	XP_011534260.1:p.Pro254=
XM_011535959.1:c.876+1558C=	XP_011534261.1:n.876+1558C=
XM_011535960.1:c.488C=	XP_011534262.1:p.Pro163=
XM_011535961.1:c.703-16697C=	XP_011534263.1:n.703-16697C=
XM_011535962.1:c.488C=	XP_011534264.1:p.Pro163=
XM_011535956.3:c.896C=	XP_011534258.1:p.Pro299=
XM_011535957.3:c.876+1558C=	XP_011534259.1:n.876+1558C=
XM_011535958.3:c.761C=	XP_011534260.1:p.Pro254=
XM_011535959.3:c.876+1558C=	XP_011534261.1:n.876+1558C=
XM_011535960.3:c.488C=	XP_011534262.1:p.Pro163=
XM_011535961.3:c.703-16697C=	XP_011534263.1:n.703-16697C=
XM_011535962.2:c.488C=	XP_011534264.1:p.Pro163=
XM_017011082.2:c.896C=	XP_016866571.1:p.Pro299=
NM_020381.4:c.896C= MANE Select	NP_065114.3:p.Pro299=