Canonical Allele Identifier: CA1653786380

Gene: PDSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107210562A= , CM000668.2:g.107210562A=	GRCh38
NC_000006.11:g.107531766A= , CM000668.1:g.107531766A=	GRCh37
NC_000006.10:g.107638459A=	NCBI36
NG_013033.1:g.254014T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369037.9:c.885T= MANE Select	ENSP00000358033.4:p.Ser295=
ENST00000369037.8:c.885T=	ENSP00000358033.4:p.Ser295=
ENST00000449027.1:c.60T=	ENSP00000392613.1:p.Ser20=
NM_020381.3:c.885T=	NP_065114.3:p.Ser295=
XM_011535956.1:c.885T=	XP_011534258.1:p.Ser295=
XM_011535957.1:c.876+1547T=	XP_011534259.1:n.876+1547T=
XM_011535958.1:c.750T=	XP_011534260.1:p.Ser250=
XM_011535959.1:c.876+1547T=	XP_011534261.1:n.876+1547T=
XM_011535960.1:c.477T=	XP_011534262.1:p.Ser159=
XM_011535961.1:c.703-16708T=	XP_011534263.1:n.703-16708T=
XM_011535962.1:c.477T=	XP_011534264.1:p.Ser159=
XM_011535956.3:c.885T=	XP_011534258.1:p.Ser295=
XM_011535957.3:c.876+1547T=	XP_011534259.1:n.876+1547T=
XM_011535958.3:c.750T=	XP_011534260.1:p.Ser250=
XM_011535959.3:c.876+1547T=	XP_011534261.1:n.876+1547T=
XM_011535960.3:c.477T=	XP_011534262.1:p.Ser159=
XM_011535961.3:c.703-16708T=	XP_011534263.1:n.703-16708T=
XM_011535962.2:c.477T=	XP_011534264.1:p.Ser159=
XM_017011082.2:c.885T=	XP_016866571.1:p.Ser295=
NM_020381.4:c.885T= MANE Select	NP_065114.3:p.Ser295=